Company : Sol Infotech Pvt. Ltd. Website : www.courtkutchehry.com DRUGS AND COSMETICS ACT, 1940 23 of 1940 [10th April, 1940] CONTENTS CHAPTER 1 :- INTRODUCTORY 1. Short title, extent and commencement 2. Application of other laws not barred 3. Definitions 3 A . Construction of references to any law not in force or any functionary not in existence in the State of Jammu and Kashmir 4. Presumption as to poisonous substances CHAPTER 2 :- T H E DRUGS TECHNICAL ADVISORY BOARD, THE CENTRAL DRUGS LABORATORY AND THE DRUGS CONSULTATIVE COMMITTEE 5. The Drugs Technical Advisory Board 6. The Central Drugs Laboratory 7. The Drugs Consultative Committee 7A. Sections 5 and 7 not to apply to Ayurvedic, Siddha or Unani drugs CHAPTER 3 :- IMPORT OF DRUGS AND COSMETICS 8. Standards of quality 9. Misbranded drugs 9A. Adulterated drugs 9B. Spurious drugs 9C. Misbranded cosmetics 9D. Spurious cosmetics 10. Prohibition of import of certain drugs or cosmetics 10A. Power of Central Government to prohibit import of drugs and cosmetics in public interest 1 1 . Application of law relating to sea customs and powers of Customs Officers 12. Power of Central Government to make rules 13. Offences 14. Confiscation 15. Jurisdiction CHAPTER 4 :- MANUFACTURE, SALE AND DISTRIBUTION OF DRUGS AND CONSMETICS 16. Standard of quality 17. Misbranded drugs 17A. Adulterated drugs 17B. Spurious drugs 17C. Misbranded cosmetics 17D. Spurious cosmetics 1 8 . Prohibition of manufacture and sale of certain drugs and cosmetics 18A. Disclosure of the name of the manufacturer, etc. 18B. Maintenance of records and furnishing of information 19. Pleas 20. Government Analysts 21. Inspectors 22. Powers of Inspectors 23. Procedure of Inspectors 24. Persons bound to disclose place where drugs or cosmetics are manufactured or kept 25. Reports of Government Analysts 2 6 . Purchaser of drugs or cosmetics enabled to obtain test or analysis 26A. Power of Central Government to prohibit manufacture, etc., of drug and cosmetic in public interest 27. Penalty for manufacture, sale, etc., of drugs in contravention of this Chapter 2 7 A . Penalty for manufacture, sale etc., of cosmetics in contravention of this Chapter 28. Penalty for non-disclosure of the name of the manufacturer, etc. 28A. Penalty for not keeping documents, etc., and for nondisclosure of information 28 B . Penalty for manufacture, etc., of drugs or cosmetics in contravention of Section 26-A 29. Penalty for use of Government Analysts report for advertising 30. Penalty for subsequent offences 31. Confiscation 31A. Application of provisions of Government departments 32. Cognizance of offences 32A. Power of Court to implead the manufacturer, etc. 33. Power of Central Government to make rules CHAPTER 4A :- PROVISIONS RELATING TO AYURVEDIC, SIDDHA AND UNANI DRUGS 33A. Chapter not to apply to Ayurvedic (including Siddha) or Unani drugs 33B. Application of Chapter IV-A 33C. Ayurvedic, Siddha and Unani Drugs Technical Advisory Board 3 3 D . T h e Ayurvedic, Siddha and Unani Drugs Consultative Committee 33E. Misbranded drugs 33EE. Adulterated drugs 33EEA. Spurious drugs 33EEB. Regulation of manufacture for sale of Ayurvedic, Siddha and Unani drugs 33EEC. Prohibition of manufacture and sale of certain Ayurvedic, Siddha and Unani drugs 33EED. Power of Central Government to prohibit manufacture, etc., of Ayurvedic, Siddha or Unani drugs in public interest 33F. Government Analysts 33G. Inspectors 33H. Application of provisions of Sections 22, 23, 24 and 25 33I. Penalty for manufacture, sale, etc., of Ayurvedic, Siddha or Unani drug in contravention of this Chapter 33J. Penalty for subsequent offences 33K. Confiscation 33L. Application of provisions to Government departments 33M. Cognizance of offences 33N. Power of Central Government to make rules 33O. Power to amend First Schedule 33P. Power to give directions CHAPTER 5 :- MISCELLANEOUS 34. Offences by companies 34A. Offences by Government departments 34AA. Penalty for vexatious search or seizure 35. Publication of sentences passed under this Act 36. Magistrates power to impose enhanced penalties 36A. Certain offences to be tried summarily 37. Protection of action taken in good faith 38. Rules to be laid before Parliament SCHEDULE 1 :- AYURVEDIC AND SIDDHA SYSTEMS SCHEDULE 2 :- STANDARDS TO BE COMPLIED WITH BY IMPORTED DRUGS AND BY DRUGS MANUFACTURED FOR SALE, SOLD, STOCKED OR EXHIBITED FOR SALE OR DISTRIBUTED DRUGS AND COSMETICS ACT, 1940 23 of 1940 [10th April, 1940] An Act to regulate the import, manufacture, distribution and sale of drugs and cosmetics Whereas it is expedient to regulate the import, manufacture, distribution and sale of drugs and cosmetics; And whereas the Legislatures of all the Provinces have passed resolutions in terms of Section 103 of the Government of India Act, 1935 (26 Geo. 5., c. 2.), in relation to such of the above-mentioned matters and matters ancillary thereto as are enumerated in List II of the Seventh Schedule to the said Act; It is hereby enacted as follows : CHAPTER 1 INTRODUCTORY 1. Short title, extent and commencement :- (1) This Act may be called the Drugs and Cosmetics Act, 1940. (2) It extends to the whole of India. (3) It shall come into force at once; but Chapter III shall take effect only from such date as the Central Government may, by notification in the Official Gazette, appoint in this behalf, and Chapter IV shall take effect in a particular State only from such date as the State Government may, by like notification, appoint in this behalf: Provided that in relation to the State of Jammu and Kashmir, Chapter III shall take effect only from such date after the commencement of the Drugs and Cosmetics (Amendment) Act, 1972 (19 of 1972), as the Central Government may, by notification in the Official Gazette, appoint in this behalf. 2. Application of other laws not barred :- The provisions of this Act shall be in addition to, and not in derogation of, the Dangerous Drugs Act, 1930 (2 of 1930), and any other law for the time being in force. 3. Definitions :- In this Act, unless there is anything repugnant in the subject or context,-- (a) "Ayurvedic, Siddha or Unani drug" includes all medicines intended for internal or external use for or in the diagnosis, treatment, mitigation or prevention of disease or disorder in human beings or animals, and manufactured exclusively in accordance with the formulae described in, the authoritative books of Ayurvdic, Sidda and Unani Tibb systems of medicine, specified in the First Schedule; (aa) "the Board" means-- (i) in relation to ayurvedic, Siddha or Unani drug, the Ayurvedic, Siddha and Unani Drugs Technical Advisory Board constituted under Section 33C; and (ii) in relation to any other drug or cosmetic, the Drugs Technical Advisory Board constituted under Section 5; (pad) "Cosmetic" means any article intended to be rubbed, poured, sprinkled or sprayed on, or introduced into, or otherwise applied to, the human body or any part thereof for cleansing, beautifying, promoting attractiveness, or altering the appearance, and includes any article intended for use as a component of cosmetic, (b) "drug" includes-- (i) all medicines for internal or external use of human beings or animals and all substances intended to be used for or in the diagnosis, treatment, mitigation or prevention of any disease or disorder in human beings or animals, including preparations applied on human body for the purpose of repelling insects like mosquitoes; (ii) such substances (other than food) intended to affect the structure or any function of the human body or intended to be used for the destruction of vermin or insects which cause disease in human beings or animals, as may be specified from time to time by the Central Government by notification in the Official Gazette; (iii) all substances intended for use as components of a drug including empty gelatin capsules; and (iv) such devices intended for internal or external use in the diagnosis, treatment, mitigation or prevention of disease or disorder in human beings or animals, as may be specified from time to time by the Central Government by notification in the official Gazette, after consultation with the Board; (c) "Government analyst" means-- (i) in relation to Ayurvedic, Siddha or Unani drug, a Government Analyst appointed by the Central Government or a State Government under Section 33-F; and (ii) in relation to any other drug or cosmetic, a Government Analyst appointed by the Central Government or a State Government under Section 21; (d) 1[* * *] (e) "Inspector" means-- (i) in relation to Ayurvedic, Siddha or Unani drug, an Inspector appointed by the Central Government or a State Government under Section 33-G; and (ii) in relation to any other drug or cosmetic, an Inspector appointed by the Central Government or a State Government under Section 21; (f) "manufacturer" in relation to any drug or cosmetic includes any process or part of a process for making, altering, ornamenting, finishing, packing, labelling, breaking up or otherwise treating or adopting any drug or cosmetic with a view to its sale or distribution but does not include the compounding or dispensing of any drug, or the packing of any drug or cosmetic, in the ordinary course of retail business; and "to manufacture" shall be construed accordingly; (g) "to import", with its grammatical variations and cognate expressions means to bring into India; (h) "patent or proprietary medicine " means,-- (i) in relation to Ayurvedic, Siddha or Unani Tibb systems of medicine all formulations containing only su ch ingredients mentioned in the formulae described in the authoritative books of Ayurveda, Siddha or Unani Tibb systems of medicine, specified in the First Schedule, but does not include a medicine which is administered by parenteral route and also a formulation included in the authoritative books as specified in clause (a); (ii) in relation to any other system of medicine, a drug which is a remedy or prescription presented in a form ready for internal or external administration of human beings or animals and which is not included in the edition of the Indian Pharmacopoeia for the time being or any other Pharmacopoeia authorised in this behalf by the Central Government after consultation with the Drugs Technical Advisory Board constituted under Section 5; (i) "Prescribed" means prescribed by rules made under this Act 1. Omitted by Act 19 of 1972. 3A. Construction of references to any law not in force or any functionary not in existence in the State of Jammu and Kashmir :- Any reference in this Act to any law which is not in force, or any functionary not in existence, in the State of Jammu and Kashmir, shall, in relation to that State, be construed as a reference to the corresponding law in force, or to the corresponding functionary in existence, in that State. 4. Presumption as to poisonous substances :- Any substance specified as poisonous by rule made under Chapter II or Chapter IV or Chapter IV-A shall be deemed to be a poisonous substance for the purposes of Chapter III or Chapter IV or Chapter IV-A, as the case may be. CHAPTER 2 THE DRUGS TECHNICAL ADVISORY BOARD, THE CENTRAL DRUGS LABORATORY AND THE DRUGS CONSULTATIVE COMMITTEE 5. The Drugs Technical Advisory Board :- (1) The Central Government shall, as soon as may be, constitute a Board (to be called the Drugs Technical Advisory Board) to advise the Central Government and the State Governments no technical matters arising out of the administration of this Act and to carry out the other functions assigned to it by this Act. (2) The Board shall consist of the following members, namely: (i) the Director General of Health Services, ex officio, who shall be Chairman; (ii) the Drugs Controller, India, ex officio; (iii) the Director of the Central Drugs Laboratory, Calcutta, ex officio; (iv) the Director of the Central Research Institute, Kasauli, ex officio; (v) the Director of the Indian Veterinary Research Institute, Izatnagar, ex officio; (vi) the President of the Medical Council of India, ex officio; (vii) the President of the Pharmacy Council of India, ex officio; (viii) the Director of the Central Drugs Research Institute, Lucknow, ex officio; (ix) two persons to be nominated by the Central Government from among persons who are in charge of drugs control in the States; (x) one person, to be elected by the Executive Committee of the Pharmacy Council of India, from among teachers in pharmacy or pharmaceutical chemistry or pharmacognosy on the staff of an Indian university or a college affiliated thereto; (xi) one person, to be elected by the Executive Committee of the Medical Council of India, from among teachers in medicine or therapeutics on the staff of an Indian university or a college affiliated thereto; (xii) one person to be nominated by the Central Government from the pharmaceutical industry; (xiii) one pharmacologist to be elected by the Governing Body of the Indian Council of Medical Research; (xiv) one person to be elected by the Central Council of the Indian Medical Association; (xv) one person to be elected by the council of the Indian Pharmaceutical Association; (xvi) two persons holding the appointment of Government Analyst under this Act, to be nominated by the Central Government (3) The nominated and elected members of the Board shall hold office for three years, but shall be eligible for re- nomination and re-election: Provided that the person nominated or elected, as the case may be, under clause (ix) or clause (x) or clause (xi) or clause (xvi) of sub-section (2) shall hold office for so long as he holds the appointment of the office by virtue of which he was nominated or elected to the Board. (4) The Board may, subject t o the previous approval of the Central Government, make bye- laws fixing a quorum and regulating its own procedure and the conduct of all business to be transacted by it. (5) The Board may constitute sub-committees and may appoint to such subcommittees for such periods, not exceeding three years, as it may decide, or temporarily for the consideration of particular matters, persons who are not members of the Board. (6) The functions of the Board may be exercised notwithstanding any vacancy therein. (7) The Central Government shall appoint a person to be Secretary of the Board and shall provide the Board with such clerical and other staff as the Central Government considers necessary. 6. The Central Drugs Laboratory :- (1) The Central Government shall, as soon as may be, establish a Central Drugs Laboratory under the control of a Director to be appointed by the Central Government, to carry out the functions entrusted to it by this Act or any rules made under this Chapter: Provided that, if the Central Government so prescribes, the functions of the Central Drugs Laboratory in respect of any drug or class of drugs or cosmetic or class of cosmetics shall be carried out at the Central Research Institute, Kasauli, or at any other prescribed Laboratory and the functions of the Director of the Central Drugs Laboratory in respect of such drug or class of drugs or such cosmetic or class of cosmetics shall be exercised by the Director of that Institute or of that other Laboratory, as the case may be. (2) The Central Government may, after consultation with the Board make rules prescribing-- (a) the functions of the Central Drugs Laboratory; (b) the procedure for the submission to the said Laboratory under Chapter IV or Chapter IV-A of samples of drugs or cosmetics for analysis or test, the forms of the Laboratorys reports thereon and the fees payable in respect of such reports; (e) such other matter as may be necessary or expedient to enable the said Laboratory to carry out its functions; (f) the matters necessary to be prescribed for the purposes of the proviso to sub-section (1). 7. The Drugs Consultative Committee :- (1) The Central Government may constitute an Advisory Committee to be called "the Drugs Consultative Committee" to advise the Central Government, the State Governments and the Drugs Technical Advisory Board on any matter tending to secure uniformity throughout India in the administration of this Act (2) The Drugs Consultative Committee shall consist of two representatives of the Central Government to be nominated by that Government and one representative of each State Government to be nominated by the State Government concerned. (3) The Drugs Consultative Committee shall meet when required to do so by the Central Government and shall have power to regulate its own procedure. 7A. Sections 5 and 7 not to apply to Ayurvedic, Siddha or Unani drugs :- Nothing contained in Sections 5 and 7 shall apply to Ayurvedic, Siddha or Unani drugs. CHAPTER 3 IMPORT OF DRUGS AND COSMETICS 8. Standards of quality :- (1) For the purposes of this Chapter, the expression "standard quality" means-- (a) in relation to a drug, that the drug complies with the standard set out in the Second Schedule, and (b) in relation to a cosmetic, that the cosmetic complies with such standard as may be prescribed. (2) The Central Government, after consultation with the Board and after giving by notification in the Official Gazette not less than three months notice of its intention so to do, may by a like notification add to or otherwise amend the Second Schedule, for the purposes of this Chapter, and thereupon the Second Schedule shall be deemed to be amended accordingly. 9. Misbranded drugs :- For the purposes of this Chapter, a drug shall be deemed to be misbranded-- (a) if it is so coloured, coated, powdered or polished that damage is concealed or if it is made to appear of better or greater therapeutic value than it really is; or (b) if it is not labelled in the prescribed manner; or (c) if its label or container or anything accompanying the drug bears any statement, design or device which makes any false claim for the drug or which is false or misleading in any particular. 9A. Adulterated drugs :- For the purposes of this Chapter, a drug shall be deemed to be adulterated,-- (a) if it consists, in whole or in part, of any filthy, putrid or decomposed substance; or (b) if it has been prepared, packed or stored under insanitary conditions whereby it may have been contaminated with filth or whereby it may have been rendered injurious to health; or (c) if its container is composed in whole or in part, of any poisonous or deleterious substance which may render the contents injurious to health; or (d) if it bears or contains, for purposes of colouring only, a colour other than one which is prescribed; or (e) if it contains any harmful or toxic substance which may render it injurious to health; or (f) if any substance has been mixed therewith so as to reduce its quality or strength. 9B. Spurious drugs :- For the purposes of this Chapter, a drug shall be deemed to be spurious-- (a) if it is imported under a name which belongs to another drug; or (b) if it is an imitation of, or is a substitute for, another drug or resembles another drug in a manner likely to deceive or bears upon it or upon its label or container the name of another drug unless it is plainly and conspicuously marked so as to reveal its true character and its lack of identity with such other drug; or (c) if the label or container bears the name of an individual or company purporting to be the manufacturer of the drug, which individual or company is fictitious or does not exist; or (d) if it has been substituted wholly or in part by another drug or substance; or (e) if it purports to be the product of a manufacturer of whom it is not truly a product. 9C. Misbranded cosmetics :- For the purposes of this Chapter, a cosmetic shall be deemed to be misbranded-- (a) if it contains a colour which is not prescribed; or (b) if it is not labelled in the prescribed manner, or (c) if the label or container or anything accompanying the cosmetic bears any statement which is false or misleading in any particular. 9D. Spurious cosmetics :- For the purposes of this Chapter, a cosmetic shall be deemed to be spurious,-- (a) if it is imported under a name which belongs to another cosmetic; or (b) if it is an imitation of, or is a substitute for, another cosmetic or resembles another cosmetic in a manner likely to deceive or bears upon it or upon its label or container the name of another cosmetic, unless it is plainly and conspicuously marked so as to reveal its true character and its lack of identity with such other cosmetic; or (c) if the label or container bears the name of an individual or a company purporting to be the manufacturer of the cosmetic which individual or company is fictitious or does not exist; or (d) if it purports to be the product of a manufacturer of whom it is not truly a product. 10. Prohibition of import of certain drugs or cosmetics :- From such date as may be fixed by the Central Government by notification in the Official Gazette in this behalf, no person shall import,-- (a) any drug or cosmetic which is not of standard quality; (b) any misbranded drug or misbranded or spurious cosmetic; (bb) any adulterated or spurious drug; (c) any drug or cosmetic for the import of which a licence is prescribed, otherwise than under, and in accordance with, such licence; (d) any patent or proprietary medicine, unless there is displayed in the prescribed manner on the label or container thereof the true formula or list of active ingredients contained in it together with the quantities thereof; (e) any drug which by means of any statement, design or device accompanying it or by any other means, purports or claims to cure or mitigate any such disease or ailment, or to have any such other effect, as may be prescribed; (ee) any cosmetic containing any ingredient which may render if unsafe or harmful for use under the directions indicated or recommended; (f) any drug or cosmetic the import of which is prohibited by rule made under this Chapter: Provided that nothing in this section shall apply to the import, subject to prescribed conditions, of small quantities of any drug for the purpose of examination, test or analysis or for personal use : Provided further that the Central Government may, after consultation with the Board, by notification in the official Gazette, permit, subject to any conditions specified in the notification, the import of any drug or class of drugs not being of standard quality. 10A. Power of Central Government to prohibit import of drugs and cosmetics in public interest :- Without prejudice to any other provision contained in this Chapter, if the Central Government is Satisfied that the use of any drug or cosmetic is likely to involve any risk to human beings or animals or that any drug does not have the therapeutic value claimed for it or contains ingredients and in such quantity for which there is no therapeutic justification and that in the public interest it is necessary or expedient so to do then, that Government may, by notification in the official Gazette, prohibit the import of such drug or cosmetic. 11. Application of law relating to sea customs and powers of Customs Officers :- (1) The law for the time being in force relating to sea customs and to goods, the import of which is prohibited by Section 18 of the Sea Customs Act, 1878 (18 of 1878) shall, subject to the provisions of Section 13 of this Act, apply in respect of drugs and cosmetics the import of which is prohibited under this Chapter, and officers of Customs and officers empowered under this Act to perform the duties imposed thereby on a Customs Collector and other officers of Customs, shall have the same powers in respect of such drugs and cosmetics as they have for the time being in respect of such goods as aforesaid. (2) Without prejudice to the provisions of sub-section (1), the Customs Collector or any officer of the Government authorized by the Central Government in this behalf, may detain any imported package which he suspects to contain any drug or cosmetic the import of which is prohibited under this Chapter and shall forthwith report such detention to the Drugs Controller, India, and, if necessary, forward the package or sample of any suspected drug or cosmetic found therein to the Central Drugs Laboratory. 12. Power of Central Government to make rules :- (1) The Central Government may, after consultation with or on the recommendation of the Board and after previous publication by notification in the official Gazette, make rules for the purpose of giving effect to the provisions of this Chapter: Provided that consultation with the Board may be dispensed with if the Central Government is of opinion that circumstances have arisen which render it necessary to make rules without such consultation, but in such a case the Board shall be consulted within six months of the making of the rules and the Central Government shall take into consideration any suggestions which the Board may make in relation to the amendment of the said rules. (2) Without prejudice to the generality of the foregoing power, such rules may-- (a) specify the drugs or classes of drugs or cosmetics or classes of cosmetics for the import of which a licence is required, and prescribe the form and conditions of such licences, the authority empowered to issue the same, the fees payable therefor and provide for the cancellation, or suspension of such licence in any case where any provision of this Chapter or the rules made thereunder is contravened or any of the conditions subject to which the licence is issued is not complied with; (b) prescribe the methods of test or analysis to be employed in determining whether a drug or cosmetic is of standard quality; (c) prescribe, in respect of biological and organometallic compounds, the units or methods of standardisation; (cc) prescribe under clause (d) of Section 9-A the colour or colours which a drug may bear or contain for purposes of colouring; (d) specify the diseases or ailments which imported drug may not purport or claim to prevent, cure or mitigate and such other effects which such drug may not purport or claim to have; (e) prescribe the conditions subject to which small quantities of drugs, the import of which is otherwise prohibited under this Chapter, may be imported for the purpose of examination, test or analysis for personal use; (f) prescribe the places at which drugs or cosmetics may be imported, and prohibit their import at any other place; (g) require the date of manufacture and the date of expiry of potency to be clearly and truly stated on the label or container of any specified imported drug or class of such drug, and prohibit the import of the said drug or class of drug after the expiry of a specified period from the date of manufacture; (h) regulate the submission by importers, and the securing, of samples of drugs or cosmetics for examination, test or analysis by the Central Drugs Laboratory, and prescribe the fees, if any, payable for such examination, test or analysis; (i) prescribe the evidence to be supplied, whether by accompanying documents or otherwise, of the quality of drugs or cosmetics sought to be imported, the procedure of officers of Customs in dealing with such evidence, and the manner of storage at places of import of drugs or cosmetics detained pending admission; (j) provide for the exemption, conditionally or otherwise from all or any of the provisions of this chapter and the rules made thereunder of drugs or cosmetics imported for the purpose only of transport through, and export from India; (k) prescribe the conditions to be observed in the packing in bottles, packages or other containers, of imported drugs or cosmetics including the use of packing material which comes into direct contact with the drugs; (l) regulate the mode of labelling drugs or cosmetics imported for sale in packages, and prescribe the matter which shall or shall not be included in such labels; (m) prescribe the maximum proportion of any poisonous substance which may be added to or contained in any imported drug, prohibit the import of any drug in which that proportion is exceeded, and specify substances which shall be deemed to be poisonous for the purposes of this Chapter and the rules made thereunder, (n) require that the accepted scientific name of any specified drug shall be displayed in the prescribed manner on the label or wrapper of any imported, patent or proprietary medicine containing such drug; (o) provide for the exemption, conditionally or otherwise, from all or any of the provisions of this Chapter or the rules made thereunder of any specified drug or class of drugs or cosmetic or class of cosmetics. 13. Offences :- (1) Whoever himself or by any other person on his behalf imports,- - (a) any drug deemed to be adulterated under Section 9-A or deemed to be a spurious drug under Section 9-B or any spurious cosmetic referred to in Section 9-D or any cosmetic of the nature referred to in clause (ee) of Section 10 shall be punishable with imprisonment for a term which may extend to three years and a fine which may extend to five thousand rupees; (b) any drug or cosmetic other than a drug or cosmetic referred to in clause (a), the import of which is prohibited under Section 10, or any rule made under this Chapter, shall be punishable with imprisonment for a term which may extend to six months, or with fine which may extend to five hundred rupees, or with both; (c) any drug or cosmetic in contravention of the provisions of any notification issued under section 10-A, shall be punishable with imprisonment for a term which may extend to three years, or with fine which may extend to five thousand rupees, or with both. (2) Whoever having been convicted of an offence-- (a) under clause (a) or clause (c) of sub-section (1), is again convicted of an offence under that clause, shall be punishable with imprisonment for a term which may extend t o five years, or with fine which may extend to ten thousand rupees, or with both; (b) under clause (b) of sub-section (1), is again convicted of an offence under that clause, shall be punishable with imprisonment for a term which may extend to one year, or with fine which may extend to one thousand rupees, or with both. (3) The punishment provided by this section shall be in addition to any penalty to which the offender may be liable under the provisions of Section 11. 14. Confiscation :- Where any offence punishable under Section 13 has been committed, the consignment of the drugs or cosmetics in respect of which the offence has been committed shall be liable to confiscation. 15. Jurisdiction :- No Court inferior to that of a Metropolitan Magistrate or of a Judicial Magistrate of the first class shall try an offence punishable under Section 13. CHAPTER 4 MANUFACTURE, SALE AND DISTRIBUTION OF DRUGS AND CONSMETICS 16. Standard of quality :- (1) For the purposes of this Chapter, the expression "standard quality" means-- (a) in relation to a drug, that the drug complies with the standard set out in the Second Schedule, and (b) in relation to a cosmetic, that the cosmetic complies such standard as may be prescribed. (2) The Central Government, after consultation with the Board and after giving by notification in the official Gazette not less than three months notice of its intention so to do, may by a like notification add to or otherwise amend the Second Schedule for the purposes of this Chapter, and thereupon the second Schedule shall be deemed to be amended accordingly. 17. Misbranded drugs :- For the purposes of this Chapter, a drug shall be deemed to be misbranded,-- (a) if it is so coloured, coated, powdered or polished that damage is concealed or if it is made to appear of better or greater therapeutic value than it really is; or (b) if it is not labelled in the prescribed manner; or (c) if its label or container or anything accompanying the drug bears any statement, design or device which makes any false claim for the drug or which is false or misleading in any particular. 17A. Adulterated drugs :- For the purposes of this Chapter, a drug shall be deemed to be adulterated,-- (a) if it consists in whole or in part, of any filth, putrid or decomposed substance; or (b) if it has been prepared, packed or stored under insanitary conditions whereby it may have been contaminated with filth or whereby it may have been rendered injurious to health; or (c) if its container is composed, in whole or in part, of any poisonous or deleterious substance which may render the contents injurious to health; or (d) if it bears or contains, for purposes of colouring only, a colour other than one which is prescribed; or (e) if it contains any harmful or toxic substance which may render it injurious to health; or (f) if any substance has been mixed therewith so as to reduce its quality or strength. 17B. Spurious drugs :- For the purpose of this Chapter, a drug shall be deemed to be spurious,-- (a) if it is manufactured under a name which belongs to another drug; or (b) if it is an imitation of, or is a substitute for, another drug or resembles another drug in a manner likely to deceive or bears upon it or upon its label or container the name of another drug unless it is plainly and conspicuously marked so as to reveal its true character and its lack of identity with such other drug; or (c) if the label or container bears the name of an individual or company purporting to the manufacturer of the drug, which individual or company is fictitious or does not exist; or (d) if it has been substituted wholly or in part by another drug or substance; or (e) if it purports to be the product of a manufacturer of whom it is not truly a product, 17C. Misbranded cosmetics :- For the purposes of this Chapter, a cosmetic shall be deemed to be misbranded,-- (a) if it contains a colour which is not prescribed; or (b) if it is not labelled in the prescribed manner; or (c) if the label or container or anything accompanying the cosmetic bears any statement which is false or misleading in any particular. 17D. Spurious cosmetics :- For the purposes of this Chapter, a cosmetic shall be deemed to be spurious,-- (a) if it is manufactured under a name which belongs to another cosmetic; or (b) if it is an imitation of, or a substitute for, another cosmetic or resembles another cosmetic in a manner likely to deceive or bears upon it or upon its label or container the name of another cosmetic unless it is plainly and conspicuously marked so as to reveal its true character and its lack of identity with such other cosmetic; or (c) if the label or container bears the name of an individual or a company purporting to be the manufacturer of the cosmetic which individual or company is fictitious or does not exist; or (d) if it purports to be the product of a manufacturer of whom it is not truly a product. 18. Prohibition of manufacture and sale of certain drugs and cosmetics :- From such date as may be fixed by the State Government by notification in the official Gazette in this behalf, no person shall himself or by any other person on his behalf-- (a) manufacture of sale or for distribution, or sell, or stock or exhibit or offer for sale, or distribute-- (i) any drug which is not of standard quality, or is misbranded, adulterated or spurious; (ii) any cosmetic which is not of a standard quality or is misbranded or spurious; (iii) any patent or proprietary medicine, unless there is displayed in the prescribed manner on the label or container thereof the true formula or list of active ingredients contained in it together with the quantities thereof; (iv) any drug which by means of any statement, design or device accompanying it or by any other means, purports or claims to prevent, cure or mitigate any such disease or ailment, or to have any such other effect as may be prescribed; (v) any cosmetic containing any ingredient which may render it unsafe or harmful for use under the directions indicated or recommended; (vi) any drug or cosmetic in contravention of any of the provisions of this Chapter or any rule made thereunder, (b) sell, or stock or exhibit or offer f o r sale, or distribute any drug or cosmetic which has been imported or manufactured in contravention of any of the provisions of this Act or any rule made thereunder; (c) manufacture for sale or for distribution, or sell, or stock or exhibit or offer for sale, or distribute any drug or cosmetic, except under, and in accordance with the conditions, of a licence issued for such purpose under this Chapter: Provided that nothing in this section shall apply to the manufacture, subject to prescribed conditions, of small quantities of any drug for the purpose of examination, test or analysis : Provided further that the Central Government may, after consultation with the Board, by notification in the official Gazette, permit, subject to any conditions specified in the notification, the manufacture for sale or for distribution, sale, stocking or exhibiting or offering for sale or distribution of any drug or class of drugs not being of standard quality. 18A. Disclosure of the name of the manufacturer, etc. :- Every person, not being the manufacturer of a drug or cosmetic or his agent for the distribution thereof, shall, if so required, disclose to the Inspector the name, address and other particulars of the person from whom he acquired the drug or cosmetic. 18B. Maintenance of records and furnishing of information :- Every person holding a licence under clause (c) of Section 18 shall keep and maintain such records, registers and other documents as may be prescribed and shall furnish to any officer or authority exercising any power or discharging any function under this Act such information as is required by such officer or authority for carrying out the purposes of this Act. 19. Pleas :- (1) Save as hereinafter provided in this section it shall be no defence in a prosecution under this Chapter to prove merely that the accused was ignorant of the nature, substance or quality of the drug or cosmetic in respect of which the offence has been committed or of the circumstances of its manufacture or import, or that a purchaser, having bought only for the purpose of test or analysis, has not been prejudiced by the sale. (2) For the purposes of Section 18 a drug shall not be deemed to be misbranded or adulterated or spurious or to be below standard quality nor shall a cosmetic be deemed to be misbranded or to be below standard quality only by reason of the fact that-- (a) there has been added thereto some innocuous substance or ingredient because the same is required for the manufacture or preparation of the drug or cosmetic as an article of commerce in a state fit for carriage or consumption, and not to increase the bulk, weight or measure of the drug or cosmetic or to conceal its inferior quality or other defects; or (b) in the process of manufacture, preparation or conveyance some extraneous substance has unavoidably become intermixed with it: provided that this clause shall not apply in relation to any sale or distribution of the drug or cosmetic occurring after the vendor or distributor became aware of such intermixture. (3) A person, not being the manufacturer of a drug or cosmetic or his agent for the distribution thereof, shall not be liable for a contravention of Section 18 if he proves-- (a) that he acquired the drug or cosmetic from a duly licensed manufacturer, distributor or dealer thereof; (b) that he did not know and could not, with reasonable diligence have ascertained that the drug or cosmetic in any way contravened the provisions of that section; and (c) that the drug or cosmetic, while in his possession, was properly stored and remained in the same state as when he acquired it 20. Government Analysts :- (1) The State Government may, by notification in the official Gazette, appoint such persons as it thinks fit, having the prescribed qualifications, to be Government Analysts for such areas in the State and in respect of such drugs or classes of drugs or such cosmetics or classes of cosmetics as may be specified in the notification. (2) The Central Government may also, by notification in the official Gazette, appoint such persons as it thinks fit, having the prescribed qualifications, to be Government Analysts in respect of such drugs or classes of drugs or such cosmetics or classes of cosmetics as may be specified in the notification. (3) Notwithstanding anything contained in sub-section (1) or sub- section (2), neither the Central Government nor a State Government shall appoint as a Government Analyst any official not serving under it without the previous consent of the Government under which he is serving. (4) No person who has any financial interest in the import, manufacture or sale of drugs or cosmetics shall be appointed to be a Government Analyst under sub-section (1) or sub-section (2) of this section. 21. Inspectors :- (1) The Central Government or a State Government may, by notification in the official Gazette, appoint such persons as it thinks fit, having the prescribed qualifications, to be Inspectors for such areas as may be assigned to them by the Central Government or the State Government, as the case may be. (2) The powers which may be exercised by a Inspector and the duties which may be performed by him, the drugs or classes of drugs or cosmetics or classes of cosmetics in relation to which and the conditions, limitations or restrictions subject to which, such powers and duties may be exercised or performed shall be such as may be prescribed. (3) No person who has any financial interest in the import, manufacture or sale of drugs or cosmetics shall be appointed to be an inspector under this section. (4) Every Inspector shall be deemed to be a public servant within the meaning of Section 21 of the Indian Penal Code (45 of 1860), and shall be officially subordinate to such authority having the prescribed qualifications, as the Government appointing him may specify in this behalf. 22. Powers of Inspectors :- (1) Subject to the provisions of Section 23 and of any rules made by the Central Government in this behalf, an Inspector may, within the local limits of the area for which he is appointed,-- (a) inspect,- - (i) any premises wherein any drug or cosmetic is being manufactured and the means employed for standardising and testing the drug or cosmetic; (ii) any premises wherein any drug or cosmetic is being sold, or stocked or exhibited or offered for sale, or distributed; (b) take samples of any drug or cosmetic,-- (i) which is being manufactured or being sold or is stocked or exhibited or offered for sale, or is being distributed; (ii) from any person who is in the course of conveying, delivering or preparing to deliver such drug or cosmetic to a purchaser or a consignee; (c) at all reasonable times, with such assistance, if any, as he considers necessary,-- (i) search any person, who, he has reason to believe, has secreted about his person, any drug or cosmetic in respect of which an offence under this Chapter has been, or is being, committed; or (ii) enter and search any place in which he has reason to believe that an offence under this Chapter has been, or is being, committed; or (iii) stop and search any vehicle, vessel or other conveyance which, he has reason to believe, is being used for carrying any drug or cosmetic in respect of which an offence under this Chapter has been, or is being, committed. and order in writing the person in possession of the drug or cosmetic in respect of which the offence has been, or is being, committed, not to dispose of any stock of such drug or cosmetic for a specified period not exceeding twenty days, or, unless the alleged offence, is such that the defect may be removed by the possessor of the drug or cosmetic, seize the stock of such drug or cosmetic and any substance or article by means of which the offence has been, or is being, committed or which may be employed for the commission of such offence; (cc) examine any record, register, document or any other material object found with any person, or in any place; vehicle, vessel or other conveyance referred to in clause (c), and seize the same if he has reason to believe that it may furnish evidence of the commission of an offence punishable under this Act or the rules made thereunder; (cca) require any person to produce any record, register, or other document relating to the manufacture for sale or for distribution, stocking, exhibition for sale, offer for sale or distribution of any drug or cosmetic in respect of which he has reason to believe that an offence under this Chapter has been, or is being, committed; (d) exercise such other powers as may be necessary for carrying out the purposes of this Chapter or any rules made thereunder. (2) The provisions of the Code of Criminal Procedure, 1973 (2 of 1974), shall, so far as may be, apply to any search or seizure under this Chapter as they apply to any search or seizure made under the authority of a warrant issued under Section 94 of the said Code. (2-A) Every record, register or other document seized under clause (cc) or produced under clause (cca) shall be returned to the person, from whom they were seized or who produce the same, within a period of twenty days of the date of such seizure or production, as the case may be, after copies thereof or extracts therefrom certified by that person, in such manner as may be prescribed, have been taken. (3) If any person wilfully obstructs an inspector in the exercise of the powers conferred upon him by or under this Chapter, or refuses to produce any record, register or other document when so required under clause (cca) of sub-section (1) he shall be punishable with imprisonment which may extend to three years, or with fine, or with both. 23. Procedure of Inspectors :- (1) Where an inspector takes any sample of a drug or cosmetic under this Chapter, he shall tender the fair price thereof and may acquire a written acknowledgment therefor. (2) Where the price tendered under sub-section (1) is refused, or where the Inspector seizes the stock of any drug or cosmetic under clause (c) of Section 22, he shall tender a receipt therefor in the prescribed form. (3) Where an inspector takes a sample of a drug or cosmetic for the purpose of test or analysis, he shall intimate such purpose in writing in the prescribed form to the person from whom he takes it and, in the presence of such person unless he wilfully absent himself, shall divide the sample into four portions and effectively seal and suitably mark the same and permit such person to add his own seal and mark to all or any of the portions so sealed and marked: Provided that where the sample is taken from premises whereon the drug or cosmetic is being manufactured, it shall be necessary to divide the sample into three portions only : Provided further that where the drug or cosmetic is made up. in containers of small volume, instead of dividing a sample as aforesaid, the inspector may, and if the drug or cosmetic be such that it is likely to deteriorate or be otherwise damaged by exposure shall, taken three or four, as the case may be, of the said containers after suitably marking the same and, where necessary, sealing them. (4) Inspector shall restore one portion of a sample so divided or one container, as the case may be, to the person from whom he takes it, and shall retain the remainder and dispose of the same as follows-- (i) one portion or container he shall forthwith send to the Government Analyst for test or analysis; (ii) the second he shall produce to the Court before which proceedings, if any, are instituted in respect of the drug or cosmetic; and (iii) the third, where taken he shall send to the person, if any, whose name, address and other particulars have been disclosed under Section 18-A. (5) Where an Inspector takes any action under clause (c) of Section 22,-- (a) he shall use all despatch in ascertaining whether or not the drug or cosmetic contravenes any of the provision of Section 18 and, if it is ascertained that the drug or cosmetic does not so contravene, forthwith revoke the order passed under the said clause or, as the case may be, take such action as may be necessary for the return of the stock seized; (b) if he seizes the stock of the drug or cosmetic, he shall as soon as may be, inform a Judicial Magistrate and take his orders as to the custody thereof; (c) without prejudice to the institution of any prosecution, if the alleged contravention be such that the defect may be remedied by the possessor of the drug or cosmetic, he shall, on being satisfied that the defect has been so remedied, forthwith revoke his order under the said clause. (6) Where an Inspector seizes any record, register, document or any other material object under clause (cc) of sub-section (1) of Section 22, he shall as soon as may be, inform a Judicial Magistrate and take his orders as to the custody thereof. 24. Persons bound to disclose place where drugs or cosmetics are manufactured or kept :- Every person for the time being in charge of any premises whereon any drug or cosmetic is being manufactured or is kept for sale or distribution shall, on being required by an Inspector so to do, be legally bound to disclose to the Inspector the place where the drug or cosmetic is being manufactured or is kept, as the case may be. 25. Reports of Government Analysts :- (1) The Government Analyst to whom a sample of any drug or cosmetic has been submitted for test or analysis under sub-section (4) of Section 23, shall deliver to the inspector submitting it a signed report in triplicate in the prescribed form. (2) The Inspector on receipt thereof shall deliver one copy of the report to the person from whom the sample was taken and another copy to the person, if any, whose name, address and other particulars have been disclosed under Section 18-A, and shall retain the third copy for use i n any prosecution in respect of the sample. (3) Any document purporting to be a report signed by a Government Analyst under this Chapter shall be evidence of the facts stated therein, and such evidence shall be conclusive unless the person from whom the sample was taken or the person whose name, address and other particulars have been disclosed under Section 18-A has, within twenty-eight days of the receipt of a copy of the report, notified in writing the Inspector or the Court before which any proceedings in respect of the sample are pending that he intends to adduce evidence in controversion of the report. (4) Unless the sample has already been tested or analysed in the Central Drugs Laboratory, where a person has under sub-section (3) notified his intention of adducing evidence in controversion of a Government Analysts report, the Court may, of its own motion or in its discretion at the request either of the complainant or the accused cause the sample of the drug or cosmetic produced before the Magistrate under sub- section (4) of Section 23 to be sent for test or analysis to the said Laboratory, which shall make the test or analysis and report in writing signed by, or under the authority of, the Director of the Central Drugs Laboratory the result thereof, and such report shall be conclusive evidence of the facts stated therein. (5) The cost of a test or analysis made by the Central Drugs Laboratory under sub- section (4) shall be paid by the complainant or accused as the Court shall direct 26. Purchaser of drugs or cosmetics enabled to obtain test or analysis :- Any person or any recognised consumer association, whether such person is a member of that association or not, shall, on application in the prescribed manner and on payment of the prescribed fee, be entitled to submit for test or analysis to a Government Analyst any drug or cosmetic purchased by him or it and to receive a report of such test or analysis signed by the Government Analyst Explanation.--For the purposes of this section and Section 32, "recognised consumer association" means a voluntary consumer association registered under the Companies Act, 1956 (1 of 1956), or any other law for the time being in force. 26A. Power of Central Government to prohibit manufacture, etc., of drug and cosmetic in public interest :- Without prejudice to any other provision contained in this chapter, if the Central Government is satisfied, that the use of any drug or cosmetic is likely to involve any risk to human beings or animals or that any drug does not have the therapeutic value claimed or purported to be claimed for it or contains ingredients and in such quantity for which there is no therapeutic justification and that in the public interest it is necessary or expedient so to do, then, that Government may, by notification in the official Gazette, prohibit the manufacture, sale or distribution of such drug or cosmetic. 27. Penalty for manufacture, sale, etc., of drugs in contravention of this Chapter :- Whoever, himself or by any other person on his behalf, manufactures for sale or for distribution, or sells, or stocks or exhibits or offers for sale or distributes,-- (a) any drug deemed to be adulterated under section 17-A or spurious under Section 17-B or which when used by any person for or in the diagnosis, treatment, mitigation, or prevention of any disease or disorder is likely to cause his death or is likely to cause such harm on his body as would amount to grievous hurt within the meaning of Section 320 of the Indian Penal Code (45 of 1860), solely on account of such drug being adulterated or spurious or not of standard quality, as the case may be, shall be punishable with imprisonment for a term which shall not be less than five years but which may extend to a term of life and with fine which shall not be less than ten thousand rupees; (b) any drug-- (i) deemed to be adulterated under Section 17-A, but not being a drug referred to in clause (a), or (ii) without a valid licence as required under clause (c) of Section 18, shall be punishable with imprisonment for a term which shall not be less than one year but which may extend to three years and with fine which shall not be less than five thousand rupees: Provided that the Court may, for any adequate and special reasons to be recorded in the judgment, impose a sentence of imprisonment for a term of less than one year and of fine of less than five thousand rupees; (c) any drug deemed to be spurious under Section 17-B, but not being a drug referred to a clause (a) shall be punishable with imprisonment for a term which shall not. be less than three years but which may extend to five years and with fine which shall not be less than five thousand rupees: Provided that the Court may, for any adequate and special reasons, to be recorded in the judgment, impose a sentence of imprisonment for a term of less than three years but not less than one year; (d) any drug, other than a drug referred to in clause (a) or clause (b) or clause (c), in contravention of any other provision of this Chapter or any rule made thereunder, shall be punishable with imprisonment for a term which shall not be less than one year but which may extend to two years and with fine: Provided that the Court may for any adequate and special reasons to be recorded in the judgment impose a sentence of imprisonment for a term of less than one year. 27A. Penalty for manufacture, sale etc., of cosmetics in contravention of this Chapter :- (i) Any cosmetic deemed to be spurious under Section 17-C shall be punishable with imprisonment for a term which may extend to three years and with fine. (ii) Any cosmetic other than a cosmetic referred to in clause (i) above in contravention of any provisions of this Chapter or any rule made thereunder shall be punishable with imprisonment for a term which may extend to one year or with fine which may extend to one thousand rupees or with both. 28. Penalty for non-disclosure of the name of the manufacturer, etc. :- Whoever contravenes the provisions of Section 18-A or Section 24 shall be punishable with imprisonment for a term which may extend to one year, or with fine which may extend to one thousand rupees, or with both. 28A. Penalty for not keeping documents, etc., and for nondisclosure of information :- Whoever without reasonable cause or excuse, contravenes the provisions of Section 18-B shall be punishable with imprisonment for a term which may extend to one year or with fine which may extend to one thousand rupees or with both. 28B. Penalty for manufacture, etc., of drugs or cosmetics in contravention of Section 26-A :- Whoever himself or by any other person on his behalf manufactures or sells or distributes any drug or cosmetic in contravention of the provisions of any notification issued under section 26-A, shall be punishable with imprisonment for a term which may extend to three years and shall also be liable to fine which may extend to five thousand rupees. 29. Penalty for use of Government Analysts report for advertising :- Whoever uses any report of a test or analysis made by the Central Drugs Laboratory or by a Government Analyst, or any extract from such report, for the purpose of advertising any drug or cosmetic, shall be punishable with fine which may extend to five hundred rupees. 30. Penalty for subsequent offences :- (1) Whoever having been convicted of an offence,-- (a) under clause (b) of Section 27 is again convicted of an offence under that clause, shall be punishable with imprisonment for a term which shall not be less than two years but which may extend to six years and with fine which shall not be less than ten thousand rupees : Provided that the Court may, for any adequate and special reasons to be mentioned in the judgment, impose a sentence of imprisonment for a term of less than two years and of fine of less than ten thousand rupees; (b) under clause (c) of Section 27 is again convicted of an offence under that clause shall be punishable with imprisonment for a term which shall not be less than six years but which may extend to ten years and with fine which shall not be less than ten thousand rupees; (c) under clause (d) of Section 27, is again convicted of an offence under that clause shall be punishable with imprisonment for a term which shall not be less than two years but which may extend to four years or with fine which shall not be less than five thousand rupees, or with both. (1- A) Whoever, having been convicted of an offence under Section 27- A is again convicted under that section, shall be punishable with imprisonment for a term which may extend to two years, or with fine which may extend to two thousand rupees, or with both. (2) Whoever, having been convicted of an offence under Section 29 is again convicted of an offence under the same Section shall be punishable with imprisonment which may extend to ten years or with fine, or with both. 31. Confiscation :- (1) Where any person has been convicted under this Chapter for contravening any such provision of this Chapter or any rule made thereunder as may be specified by rule made in this behalf, the stock of the drug or cosmetic in respect of which the contravention has been made shall be liable to confiscation and if such contravention is in respect of -- (i) manufacture of any drug deemed to be misbranded under Section 17, adulterated under Section 17-A or spurious under Section 17-B; or (ii) manufacture for sale, or for distribution, sale, or stocking or exhibiting or offering for sale, or distribution of any drug without a valid licence as required under clause (c) of Section 18, any implements or machinery used in such manufacture, sale or distribution and any receptacles, packages or covering in which such drug is contained and the animals, vehicles, vessles or other conveyances used in carrying such drug shall also be liable to confiscation. (2) Without prejudice to the provisions contained in sub-section (1), where the Court is satisfied, on the application of an Inspector or otherwise and after such inquiry as may be necessary that the drug or cosmetics is not of standard quality or is a misbranded, adulterated or spurious drug or misbranded or spurious cosmetic, such drug or, as the case may be, such cosmetic shall be liable to confiscation. 31A. Application of provisions of Government departments :- The provisions of this Chapter except those contained in Section 31 shall apply in relation to the manufacture, sale or distribution of drugs by any department of Government as they apply in relation to the manufacture, sale or distribution of drugs by any other person. 32. Cognizance of offences :- (1) No prosecution under this Chapter shall be instituted except by an Inspector or by the person aggrieved or by a recongnised consumer association whether such person is a member of that association or not. (2) No Court inferior to that of a Metropolitan Magistrate or of a Judicial Magistrate of the first class shall try an offence punishable under this Chapter. (3) Nothing contained in this Chapter shall be deemed to prevent any person from being prosecuted under any other law for any act or omission which constitutes an offence against this Chapter. 32A. Power of Court to implead the manufacturer, etc. :- Where at any time during the trial of any offence under this Chapter alleged to have been committed by any person, not being the manufacturer of a drug or cosmetic or his agent for the distribution thereof, the Court is satisfied, on the evidence adduced before it, that such manufacturer or agent is also concerned in that offence, then, the Court may, notwithstanding anything contained in sub-sections (1), (2) and (3) of Section 319 of the Code of Criminal Procedure, 1973 (2 of 1974), proceed against him as though a prosecution had been instituted against him under Section 32. 33. Power of Central Government to make rules :- (1) The Central Government may after consultation with or on the recommendation of the Board and after previous publication by notification in the official Gazette, make rules for the purpose of giving effect to the provisions of this Chapter : Provided that consultation with the Board may be dispensed with if the Central Government is of opinion that circumstances have arisen which render it necessary to make rules without such consultation, but in such a case the Board shall be consulted within six months of the making of the rules and the Central Government shall take into consideration any suggestions which the Board may make in relation to the amendment of the said rules. (2) Without prejudice to the generality of the foregoing power, such rule may-- (a) provide for the establishment of laboratories for testing and analysing drugs or cosmetics; (b) prescribe the qualifications and duties of Government Analysts and the qualifications of Inspectors; (c) prescribe the methods of test or analysis to be employed in determining whether a drug or cosmetic is of standard quality; (d) prescribe, in respect of biological and organometallic compounds, the units or methods of standardisation; (dd) prescribe under clause (d) of Section 17-A the colour or colours which a drug may bear or contain for purposes of colouring; (e) prescribe the forms of licences for the manufacture for sale or for distribution, for the sale and for the distribution of drugs or any specified drug or class of drugs or of cosmetics or any specified cosmetic or class of cosmetics, the form of application for such licences, the conditions subject to which such licences may be issued, the authority empowered to issue the same the qualifications of such authority and the fees payable therefor and provide for the cancellation or suspension of such licences in any case where any provision of this Chapter or the rule made thereunder is contravened or any of the conditions subject to which they are issued is not complied with ; (ee) prescribe the records, registers or other documents to be kept and maintained under Section 18-B; (eea) prescribe the fees for the inspection (for the purposes of grant or renewal of licences) of premises, wherein any drug or cosmetic is being or is proposed to be manufactured; (eeb) prescribe the manner in which copies are to be certified under sub-section (2-A) of Section 22; (f) specify the diseases or ailments which a drug may not purport or claim to prevent, cure or mitigate and such other effects which a drug may not purport or claim to have; (g) prescribe the conditions subject to which small quantities of drugs may be manufactured for the purpose of examination, test or analysis; (h) require the date of manufacture and the date of expiry of potency to be clearly and truly stated on the label or container of any specified drug or class of drugs, and prohibit the sale, stocking or exhibition for sale, or distribution of the said drug or class of drugs after the expiry of a specified period from the date of manufacture or after the expiry of the date of potency; (i) prescribe the conditions to be observed in the packing in bottles, packages, and other containers of drugs or cosmetics including the use of packing material which comes into direct contact with the drugs, and prohibit the sale, stocking or exhibition for sale, or distribution of drugs or cosmetics packed in contravention of such conditions; (j) regulate the mode of labelling [packed drugs or cosmetics], and prescribe the matter which shall or shall not be included in such labels; (k) prescribe the maximum proportion of any poisonous substance which may be added to or contained in any drug, prohibit the manufacture, sale or stocking or exhibition for sale, or distribution of any drug in which that proportion is exceeded, and specify substances which shall be deemed to be poisonous for the purposes of this Chapter and the rules made thereunder; (l) require that the accepted scientific name of any specified drug shall be displayed in the prescribed manner on the label or wrapper of any patent or proprietary medicine containing such drug; (m) 1[* * *] (n) prescribe the powers and duties of Inspectors and the qualifications of the authority to which such Inspectors shall be subordinate and specify the drugs or classes of drugs or cosmetics or classes of cosmetics in relation to which and the conditions, limitations or restrictions subject to which, such powers and duties may be exercised or performed; (o) prescribe the forms of report to be given by Government Analysts, and the manner of application for test or analysis under Section 56 and the fees payable therefor, (p) specify the offences against this Chapter or any rule made thereunder in relation to which an order of confiscation may be made under Section 31; and (q) provide for the exemption, conditionally or otherwise, from all or any of the provisions of this Chapter or the rules made thereunder, of any specified drug or class of drugs or cosmetic or class of cosmetics; 1. Omitted by Act 13 of 1964. CHAPTER 4A PROVISIONS RELATING TO AYURVEDIC, SIDDHA AND UNANI DRUGS 33A. Chapter not to apply to Ayurvedic (including Siddha) or Unani drugs :- Save as otherwise provided in this Act, nothing contained in this Chapter shall apply to Ayurvedic (including Siddha) or Unani drugs. 33B. Application of Chapter IV-A :- This Chapter shall apply only to Ayurvedic, Siddha and Unani Drugs. 33C. Ayurvedic, Siddha and Unani Drugs Technical Advisory Board :- (1) The Central Government shall, by notification in the official Gazette and with effect from such date as may be specified therein, constitute a Board (to be called the Ayurvedic, Siddha and Unani Drugs Technical Advisory Board) to advise the Central Government and the State Governments on technical matters arising out of this Chapter and to carry out the other functions assigned to it by this Chapter. (2) The Board shall consist of the following members, namely : (i) The Director General of Health Services, ex officio; (ii) the Drugs Controller, India, ex officio; (iii) the principal officer dealing with Indian systems of medicine in the Ministry of Health, ex officio; (iv) the Director of the Central Drugs Laboratory, Calcutta, ex officio; (v) one person holding the appointment of Government Analyst under Section 34-F, to be nominated by the Central Government; (vi) one Pharmacognocist to be nominated by the Central Government; (vii) one Photo-chemist to be nominated by the Central Government; (viii) four persons to be nominated by the Central Government, two from amongst the members of the Ayurvedic Pharmacopoeia Committee, one from amongst the members of the Unani Pharmacopoeia Committee and one from amongst the members of the Siddha Pharmacopoeia Committee; (ix) one teacher in Darvyaguna, and Bhaishjya Kalpana, to be nominated by the Central Government; (x) one teacher in ILM-UL- ADVIA and TAKLIS-WADAWASAZI, to be nominated by the Central Government; (xi) one teacher in Gunapadam to be nominated by the Central Government; (xii) three persons, one each to represent the Ayurvedic, Siddha and Unani drug industry, to be nominated by the Central Government; (xiii) three persons, one each from among the practitioners of Ayurvedic, Siddha and Unani Tibb systems of medicine to be nominated by the Central Government (3) The Central Government shall appoint a member of the Board as its Chairman. (4) The nominated members of the Board shall hold office for three years but shall be eligible for renomination. (5) The Board may, subject to the previous approval of the Central Government, make bye-laws fixing a quorum and regulating its own procedure and conduct of all business to be transacted by it (6) The functions of the Board may be exercised notwithstanding any vacancy therein. (7) The Central Government shall appoint a person to be Secretary of the Board and shall provide the Board with such clerical and other staff as the Central Government considers necessary. 33D. The Ayurvedic, Siddha and Unani Drugs Consultative Committee :- (1) The Central Government may constitute an Advisory Committee to be called the Ayurvedic, Siddha and Unani Drugs Consultative Committee to advise the Central Government, the State Governments and the Ayurvedic, Siddha and Unani Drugs Technical Advisory Board on any matter for the purpose as securing uniformity throughout India in the administration of this Act in so far as it relates to Ayurvedic, Siddha or Unani drugs. (2) The Ayurvedic, Siddha and Unani Drugs Consultative Committee shall consist of two persons to be nominated by the Central Government a s representatives of that Government and not more than one representative of each State to be nominated by the State Government concerned. (3) The Ayurvedic, Siddha and Unani Durgs consultative Committee shall meet when required to do so by the Central Government and shall regulate its own procedure 33E. Misbranded drugs :- For the purposes of this Chapter, an Ayurvedic, Siddha or Unani drug shall be deemed to be misbranded-- (a) if it is so coloured, coated, powdered or polished that damage is concealed, or if it is made to appear of better or greater therapeutic value than it really is; or (b) if it is not labelled in the prescribed manner; or (c) if its label or container or anything accompanying the drug bears any statement, design or device which makes any false claim for the drug or which is false or misleading in any particular. 33EE. Adulterated drugs :- For the purposes of this Chapter, an Ayurvedic, Siddha or Unani drug shall be deemed to be adulterated,-- (a) if it consists, in whole or in part, of any filthy, putrid or decomposed substance; or (b) if it has been prepared, packed or stored under insanitary conditions whereby it may have been contaminated with filth or whereby it may have been rendered injurious to health; or (c) if its container is composed, in whole or in part, of any poisonous or deleterious substance which may render the contents injurious to health; or (d) if it bears or contains, for purposes of colouring only, a colour other than one which is prescribed; or (e) if it contains any harmful or toxic substance which may render it injurious to health; or (f) if any substance has been mixed therewith so as to reduce its quality or strength. Explanation.-- For the purpose of clause (a), a drug shall not be deemed to consist in whole or in part, of any decomposed substance only by reason of the fact that such decomposed substance is the result of any natural decomposition of the drug: Provided that such decomposition is not due to any negligence on the part of the manufacturer of the drug or the dealer thereof and that it does not render the drug injurious to health. 33EEA. Spurious drugs :- For the purposes of this Chapter, an Ayurvedic, Siddha or Unani Drug shall be deemed to be spurious-- (a) if it is sold, or offered or exhibited for sale, under a name which belongs to another drug; or (b) if it is an imitation of, or is a substitute for, another drug or resembles another drug in a manner likely to deceive, or bears upon it or upon its label or container the name of another drug, unless it is plainly and conspicuously marked so as to reveal its true character and its lack of identity with such other drug; or (c) if the label or container bears the name of an individual or company purporting to be the manufacturer of the drug, which individual or company is fictitious or does not exist; or (d) if it has been substituted wholly or in part by any other drug or substance; or (e) if it purports to be the product of a manufacturer of whom it is not truly a product. 33EEB. Regulation of manufacture for sale of Ayurvedic, Siddha and Unani drugs :- No person shall manufacture for sale or for distribution any Ayurvedic, Siddha or Unani drug except in accordance with such standards, if any, as may be prescribed in relation to that drug. 33EEC. Prohibition of manufacture and sale of certain Ayurvedic, Siddha and Unani drugs :- From such date as the State Government may, by notification in the official Gazette, specify in this behalf, no person, either by himself or by any other person on his behalf, shall-- (a) manufacture for sale or for distribution-- (i) any misbranded, adulterated or spurious Ayurvedic, Siddha or Unani durg; (ii) any patent or proprietary medicine, unless there is displayed in the prescribed manner on the label or container thereof the true list of all the ingredients contained in it; and (iii) any Ayurvedic, Siddha or Unani drug in contravention of any of the provisions of this Chapter or any rule made thereunder; (b) sell, stock or exhibit or offer for sale or distribute any Ayurvedic, Siddha or Unani drug which has been manufactured in contravention of any of the provisions of this Act, or any rule made thereunder; (c) manufacture for sale or for distribution, any Ayurvedic, Siddha or Unani drug, except under, and in accordance with the conditions of, a licence issued for such purpose under this Chapter by the prescribed authority: Provided that nothing in this section shall apply to Vaidyas and Hakims who manufacture Ayurvedic, Siddha or Unani drug for the use of their own patients: Provided further that nothing in this section shall apply to the manufacture, subject to the prescribed conditions, of small quantities of any Ayurvedic, Siddha or Unani drug for the purpose of examination, test or analysis. 33EED. Power of Central Government to prohibit manufacture, etc., of Ayurvedic, Siddha or Unani drugs in public interest :- Without prejudice to any other provisions contained in this Chapter, if the Central Government is satisfied on the basis of any evidence or other material available before it that the use of any Ayurvedic, Siddha or Unani drug is likely to involve any risk to human beings or animals or that any such drug does not have the therapeutic value claimed or purported to be claimed for it and that in the public interest it is necessary or expedient so to do then, that Government may, by notification in the official Gazette, prohibit the manufacture, sale or distribution of such drug. 33F. Government Analysts :- (1) The Central Government may, by notification in the official Gazette, appoint such persons as it thinks fit having the prescribed qualifications to be Government Analysts for such areas as may be assigned to them by the Central Government or the State Government, as the case may be. (2) Notwithstanding anything contained in sub-section (1), neither the Central Government nor a State Government shall appoint as a Government Analyst any official not serving under it without the previous consent of the Government under which he is serving. (3) No person who has any financial interest in the manufacture or sale of any drug shall be appointed to be a Government Analyst under this section. 33G. Inspectors :- (1) The Central Government or a State Government may, by notification in the official Gazette, appoint such persons as it thinks fit, having the prescribed qualification, to be Inspectors for such areas as may be assigned to them by the Central Government or the State Government as the case may be. (2) The powers which may be exercised by an Inspector and the duties which may be performed by him and the conditions, limitations or restrictions subject to which such powers and duties may be exercised or performed shall be such as may be prescribed. (3) No person who has any financial interest in the manufacture or sale of any drug shall be appointed to be an Inspector under this section. (4) Every Inspector shall be deemed to be a public servant within the meaning of Section 21 of the Indian Penal Code (45 of 1860) and shall be officially subordinate to such authority as the Government appointing him may specify in this behalf. 33H. Application of provisions of Sections 22, 23, 24 and 25 :- The provisions of Sections 22, 23, 24 and 25 and the rules, if any, made thereunder shall, so far as may be, apply in relation to an Inspector and a Government Analyst appointed under this Chapter as they apply in relation to an inspector and a Government Analyst appointed under Chapter IV, subject to the modification that the references to "drug" in the said sections, shall be construed as reference to "Ayurvedic, Siddha or Unani drug". 33I. Penalty for manufacture, sale, etc., of Ayurvedic, Siddha or Unani drug in contravention of this Chapter :- Whoever himself or by any other person on his behalf-- (1) manufactures for sale or for distribution,-- (a) any Ayurvedic, Siddha or Unani drug-- (i) deemed to be adulterated under Section 33-EE, or (ii) without a valid licence as required under clause (c) of section 33-EEC, shall be punishable with imprisonment for a term which may extend to one year and with fine which shall not be less than two thousand rupees; (b) any Ayurvedic, Siddha or Unani drug deemed to be spurious under Section 33-EEA, shall be punishable with imprisonment for a term which shall not be less than one year but which may extend to three years and with fine which shall not be less than five thousand rupees : Provided that the Court may, for any adequate and special reasons to be mentioned in the judgment, impose a sentence of imprisonment for a term of less than one year and of fine of less than five thousand rupees; or (2) contravenes any other provisions of this Chapter or of Section 24 as applied by Section 33-H or any rule made under this Chapter, shall be punishable with imprisonment for a term which may extend to three months and with fine which shall not be less than five thousand rupees. 33J. Penalty for subsequent offences :- Whoever having been convicted of an offence,-- (a) under clause (a) of sub-section (1) of Section 33-1 is again convicted of an offence under that clause, shall be punishable with imprisonment for a term which may extend to two years and with fine which shall not be less than two thousand rupees; (b) under clause (b) of sub- section (1) of Section 33-1 is again convicted of an offence under that clause, shall be punishable with imprisonment for a term which shall not be less than two years but which may extend to six years and with fine which shall not be less than five thousand rupees : Provided that the court may, for any adequate and special reasons to be mentioned in the judgment, impose a sentence of imprisonment for a term of less than two years and of fine of less than five thousand rupees; (c) under sub-section (2) of Section 33- I is again convicted of an offence under that sub-section, shall be punishable with imprisonment for a term which may extend to six months and with fine which shall not be less than one thousand rupees. 33K. Confiscation :- Where any person has been convicted under this Chapter, the stock of the Ayurvedic, Siddha or Unani drug, in respect of which the contravention has been made, shall be liable to confiscation. 33L. Application of provisions to Government departments :- The provisions of this Chapter except those contained in Section 33-K shall apply in relation to the manufacture for sale, sale or distribution of any Ayurvedic, Siddha or Unani drug by any department of Government as they apply in relation to the manufacture for sale, sale or distribution of such drug by any other person. 33M. Cognizance of offences :- (1) No prosecution under this Chapter shall be instituted except by an Inspector with the previous sanction of the authority specified under sub-section (4) of Section 33-G. (2) No Court inferior to that of a Metropolitan Magistrate or of a Judicial Magistrate of the first class shall try any offence punishable under this Chapter. 33N. Power of Central Government to make rules :- (1) The Central Government may after consultation with, or on the recommendation of, the Board and after previous publication by notification in the official Gazette, make rules for the first purpose of giving effect to the provisions of this Chapter: Provided that consultation with the Board may be dispensed with if the Central Government is of opinion that circumstances have arisen which render it necessary to make rules without such consultation, but in such a case, the Board shall be consulted within six months of the making of the rules and the Central Government shall take into consideration any suggestions which the Board may make in relation to the amendment of the said rules. (2) Without prejudice to the generality of the foregoing power, such rules may-- (a) provide for the establishment of laboratories for testing and analysing Ayurvedic, Siddha or Unani drugs; (b) prescribe the qualifications and duties of Government Analysts and the qualifications of Inspectors; (c) prescribe the methods of test or analysis to be employed in determining whether any Ayurvedic, Siddha or Unani drug is labelled with the true list of the ingredients which it is purported to contain; (d) specify any substance as a poisonous substance; (e) prescribe the forms of licences for the manufacture for sale of Ayurvedic, Siddha or Unani drug and for sale of processed Ayurvedic, Siddha or Unani drugs, the form of application for such licences, the conditions subject to which such licences may be issued, the authority empowered to issue the same and the fees payable therefor and provide for the cancellation or suspension of such licences in any case where any provision of this Chapter or rules made thereunder is contravened or any of the conditions subject to which they are issued is not complied with; (f) prescribe the conditions to be observed in the packing of Ayurvedic, Siddha and Unani drugs including the use of packing material which comes into direct contact with the drugs, regulate the mode of labelling, packed drugs and prescribe the matters which shall not be included in such labels; (g) prescribe the conditions subject to which small quantities of Ayurvedic, Siddha or Unani drugs may be manufactured for the purpose of examination, test or analysis; (gg) prescribe under clause (d) of Section 33-EE the colour or colours which an Ayurvedic, Siddha or Unani drug may bear or contain for purposes of colouring ; (gga) prescribe the standards for Ayurvedic, Siddha or Unani drugs under Section 33-EEB; and (h) any other matter which is to be or may be prescribed under this Chapter. 33O. Power to amend First Schedule :- The Central Government, after consultation with the Board and after giving, by notification in the official Gazette, not less than three months notice of its intention so to do, may, by a like notification, add to or otherwise amend the First Schedule for the purpose of this Chapter and thereupon the said Schedule shall be deemed to be amended accordingly. 33P. Power to give directions :- The Central Government may give such directions to any State Government as may appear to the Central Government to be necessary for carrying into execution in the State any of the provisions of this Act or of any rule or order made thereunder. CHAPTER 5 MISCELLANEOUS 34. Offences by companies :- (1) Where an offence under this Act has been committed by a company, every person who at the time the offence was committed, was in charge of, and was responsible to the company for the conduct of the business of the company, as well as the company shall be deemed to be guilty of the offence and shall be liable to be proceeded against the punished accordingly : Provided that nothing contained in this sub-section shall render any such person liable to any punishment provided in this Act if he proves that the offence was committed without his knowledge or that he exercised all due diligence to prevent the commission of such offence. (2) Notwithstanding anything contained in sub-section (1), where an offence under this Act has been committed by a company and it is proved that the offence has been committed with the consent or connivance of, or is attributable to any neglect on the part of, any Director, Manager, Secretary or other Officer of the company, such director, manager, secretary or other officer shall also be deemed to be guilty of that offence and shall be liable to be proceeded against and punished accordingly. Explanation.--For the purpose of this section-- (a) "company" means a body corporate, and includes a firm or other association of individuals; and (b) "director" in relation to a firm means a partner in the firm. 34A. Offences by Government departments :- Where an offence under Chapter IV or Chapter IV-A has been committed by any department of Government, such authority as is specified by the Central Government to be in charge of manufacture, sale or distribution of drugs or where no authority is specified, the head of the department, shall be deemed to be guilty of the offence and shall be liable to be proceeded against and punished accordingly: Provided that nothing contained in this section shall render any such authority or person liable to any punishment provided in Chapter IV or Chapter IV-A, as the case may be, if such authority or person proves that the offence was committed without its or his knowledge or that such authority or person exercised all due diligence to prevent the commission of such offence. 34AA. Penalty for vexatious search or seizure :- Any Inspector exercising powers under this Act or the rules made thereunder, who,-- (a) without reasonable ground of suspicion, searches any place, vehicle, vessel or other conveyance; or (b) vexatiously and unnecessarily searches any person; or (c) vexatiously and unnecessarily seizes any drug or cosmetic, or any substance or article, or any record, register, document or other material object; or (d) commits, as such Inspector, any other act, to the injury of any person without having reason to believe that such act is required for the execution of his duty, shall be punishable with fine which may extend to one thousand rupees. 35. Publication of sentences passed under this Act :- (1) If any person is convicted of an offence under this Act, the Court before which the conviction takes place shall, on application made to it by the Inspector, cause the offenders name, place of residence, the offence of which he has been convicted and the penalty which has been inflicted upon him, to be published at the expense of such person in such newspapers or in such other manner as the Court may direct. (2) The expenses of such publication shall be deemed to form part of the costs relating to the conviction and shall be recoverable in the same manner as those costs are recoverable. 36. Magistrates power to impose enhanced penalties :- Notwithstanding anything contained in the Code of Criminal Procedure, 1973 (2 of 1974), it shall be lawful for any Metropolitan Magistrate or any Judicial Magistrate of the first class to pass any sentence authorized by this Act in excess of his powers under the said Code. 36A. Certain offences to be tried summarily :- Notwithstanding anything contained in the Code of Criminal Procedure, 1973 (2 of 1974), all offences under this Act, punishable with imprisonment for a term not exceeding three years, other than an offence under clause (b) of sub-section (1) of Section 33-1, shall be tried in a summary way by a Judicial Magistrate of the first class specially empowered in this behalf by the State Government or by a Metropolitan Magistrate and the provisions of Sections 262 to 265 (both inclusive) of the said Code shall, as far as may be, apply to such trial: Provided that, in the case of any conviction in a summary trial under this section, it shall be lawful for the Magistrate to pass a sentence of imprisonment for a term not exceeding one year: Provided further that when at the commencement of, or in the course of, a summary trial under this section it appears to the Magistrate that the nature of the case is such that a sentence of imprisonment for a term exceeding one year may have to be passed or that it is, for any other reason, undesirable to try the case summarily, the Magistrate shall, after hearing the parties, record an order to that effect and thereafter recall any witness who has been examined and proceed to hear or rehear the case in the manner provided by the said Code. 37. Protection of action taken in good faith :- No suit, prosecution or other legal proceedings shall lie against any person for anything which is in good faith done or intended to be done under this Act. 38. Rules to be laid before Parliament :- Every rule made under this Act shall be laid as soon as may be after it is made before each House of Parliament while it is in session for a total period of thirty days which may be comprised in one session or in two or more successive sessions, and, if, before the expiry of the session immediately following the session or the successive sessions aforesaid, both Houses agree in making any modification in the rule or both houses agree that the rule should not be made, the rule shall thereafter have effect only in such modified form or be of no effect, as the case may be; so however that any such modification or annulment shall be without prejudice to the validity of anything previously done under that rule. SCHEDULE 1 AYURVEDIC AND SIDDHA SYSTEMS [See Section 3 (a)] Serial No. Name of books Ayurveda 1 Arogya Kalpadruma 2 Arka Prakasha 3 Arya Bhishak 4 Ashtanga Hridaya 5 Ashtanga Samgraha 6 Ayurveda Kalpadruma 7 Ayurveda Prakasha 8 Ayurveda Samgraha 9 Bhaishajya Ratanavali 10 Bharat Bhaishajya Ratnakara 11 Bhava Prakasha 12 Brihat Nighantu Ratnakara 13 Charaka Samhita 14 Chakra Datta 15 Gada Nigraha 16 Kupi Pakva Rasayana 17 Nighantu Ratnakara 18 Rasa Chandanshu 19 Rasa Raja Sundara 20 Rasaratna Samuchaya 21 Rasatantra Sara Siddha Prayoga Samgraha 22 Rasa Tarangini 23 Rasa Yoga Sagara 24 Rasa Yoga Ratnakara 25 Rasa Yoga Samgraha 26 Rasendra Sara Samgraha 27 Rasa Pradipika 28 Sahasrayoga 29 Sarvaroga Chikitsa Ratnam 30 Sarvayoga Chikitsa Ratnam 31 Sharangadhara Samhita 32 Siddha Bhaishajya Manimala 33 Siddha Yoga Samgraha 34 Sushruta Samhita 35 Vaidya Chintamani 36 Vaidyaka Shabda Sindu 37 Vaidyaka Chikitsa Sara 38 Vaidya Jiwan 39 Basava Rajeeyam 40 Yoga Ratnakara 41 Yoga Tarangini 42 Yoga Chintamani 43 Kashyapasamhita 44 Bhelasamhita 45 Vishwanathachikitsa 46 Vrindachikitsa 47 Ayurvedachintamani 48 Abhinavachintamani 49 Ayurveda-ratnakar 50 Yogarantnasangraha 51 Rasamrita 52 Dravyagunanighantu 53 Rasamanjari 54 Bangasena 1[54-A Ayurvedic Formulary of India (Part I) 54-B Ayurveda Sara Samgraha] Siddha 55 Siddha Vaidya Thirattu 56 Therayar Maha Karisal 57 Brahma Muni Karukkadai (300) 58 Bhogar (700) 59 Pulippani (500) 60 Agaslhiya Paripuranam (400) 61 Thcraya Yamagam 62 Agasthiyar Chcnduram (300) 63 Agasthiyar (500) 64 Athmarakshamrutham 65 Agasthiyar Pin (80) 66 Agasthiyar Rathna Churukkam 67 Thcraya Karisal (300) 68 Vccramamuni Nasa Kandam 69 Agasthiyar (600) 70 Agasthiyar Kanma Soothiram 71 18 Siddhars Chillarai Kovai 72 Yogi Vatha Kaviyam 73 Thcrayar Tharu 74 Agasthiyar Vaidya Kaviyam (1500) 75 Bala Vagadam 76 Chimittu Rathna (Rathna) Churukkam 77 Nagamuni (200) 78 Agasthiyar Chillarai Kovai 79 Chikicha Rathna Deepam 80 Agasthiyar Nayana Vidhi 81 Yugu Karisan (151) 82 Agasthiyar Vallathi (600) 83 Therayar Thaila Varkam 1[84 Siddha Formulary of India (Part I)] B.--UNANI TIBB SYSTEM 1 Karabadin Qadri 2 Karabadin Kabir 3 Karabadin Azam 4 IIaj-ul-Amraz 5 Al Karabadin 6 Biaz Kabir, Vol. II 7 Karabadin Jadid 8 Kitab-ul-Taklis 9 Sanat-ul-Taklis 10 Mifta-ul-Khazain 11 Madan-ul-Aksir 12 Makhzan-ul-Murabhat 1[13 National Formulary of Unani Medicine (Part I)] SCHEDULE 2 STANDARDS TO BE COMPLIED WITH BY IMPORTED DRUGS AND BY DRUGS MANUFACTURED FOR SALE, SOLD, STOCKED OR EXHIBITED FOR SALE OR DISTRIBUTED [See Sections 8 and 16] Class of drug Standard to be complied with 1 . Patent or proprietary medicines other than Homoeopathic medicines. The formula or list of ingredients displayed in the prescribed manner on the label or container and such other standards as may be prescribed. 1[2. Substances commonly known as vaccines, sera, toxins, toxoids, antitoxins and antigens and biological products of like nature, for human use or for veterinary use. 3. 2[* * *] The standards maintained at the International Laboratory for Biological Standards, Stantans Serum Institute, Copenhagen and at the Central Veterinary Laboratory, Weybridge Surrey, U.K., and such other laboratories recognised by the Word Health Organisation from time to time, and such further standards of strength, quality, and purity, as may be prescribed.] 4. Substances (other than food) intended to affect the structure or any function of the human body or intended to be used for the destruction of vermin or insects which cause disease in human beings or animals. Such standards as may be prescribed. 4-A. Homoeopathic medicines: (a) Drugs included in the Homoeopathic Pharmacopoeia of India. Standards of identity, purity and strength specified in the edition of the Homoeopathic Pharmacopoeia of India for the time being and such other standards as may be prescribed. Class of drug Standard to be complied with (b) Drugs not included in the Homoeopathic Pharmacopoeia of India but which are included in the Homoeopathic Pharmacopoeia of the United States of America or the United Kingdom or the German Homoeopathic Pharmacopoeia. Standards of identity, purity and strength prescribed for the Drugs in the edition of such Pharmacopoeia for the time being in which they are given and such other standards as may be prescribed. (c) Drugs not included in the Homoeopathic Pharmacopoeia of India or the United States of America or the United Kingdom or the German Homoeopathic Pharmacopoeia. The formula or list of ingredients displayed in the prescribed manner on the label of the container and such other standards as may be prescribed by the Central Government. 5. Other drugs : (a) Drugs included in the Indian Pharmacopoeia. Standards of identity, purity and strength specified in the edition of the Indian Pharmacopoeia for the time being and such other standards as may be prescribed. (b) Drugs not included in the Indian Pharmacopoeia but which are included in any Pharmacopoeia of any other country. Standards of identity, purity and strength specified for the drugs in the edition such of Pharmacopoeia for the time being and such other standards as may be prescribed. 1. Substituted by G.S.R. 299 (E), dated 23rd April, 1984. 2. Omitted by G.S.R. 299 (E), dated 23rd April, 1984