The DRUGS AND COSMETICS ACT AND RULES
punjab · 1940
- S. 1General Principles: Toxicity studies should comply with the norms of Good Laboratory Practice (GLP)
- S. 2—
- S. 3—
- S. 3AConstruction of references to any law not in force or any functionary not in existence in the State of Jammu and Kashmi
- S. 4Subs
- S. 5Method of testing - (1) Preparation of sample
- S. 5A—
- S. 6Amended by G
- S. 7—
- S. 7ASections 5 and 7 not to apply to Ayurvedic, Siddha or Unani drugs
- S. 8Plant concentrates/ extracts and exudates/resins
- S. 9Subs
- S. 9AAdulterated drugs
- S. 9BSpurious drugs
- S. 9CMisbranded cosmetics
- S. 9DSpurious cosmetics
- S. 10Form-Fill-Seal Technology or Blow, Fill-Seal Technology: 10
- S. 10APower of Central Government to prohibit import of drugs and cosmetics in public interest
- S. 11—
- S. 12Subs
- S. 132[The following household remedies, namely:– 3[(1) Asprin Tablets
- S. 14—
- S. 15Standards for other mechanical contraceptive - Standards for ‘Copper T’ and ‘Tubal Ring’ shall be as laid down in Annex
- S. 16Quality Control System
- S. 17Specification 17
- S. 17AAdulterated drugs
- S. 17BSpurious drugs
- S. 17CMisbranded cosmetics
- S. 17DSpurious cosmetics
- S. 18Prohibition of manufacture and sale of certain drugs and cosmetics
- S. 18ADisclosure of the name of the manufacturer, etc
- S. 18BMaintenance of records and furnishing of information
- S. 19Pleas
- S. 20Batch Packaging Records: 20
- S. 21Batch Processing Records 21
- S. 22Standard Operating Procedures (SOPs) and Records, regarding: 22
- S. 23Needle destroyer (wherever necessary)
- S. 24Persons bound to disclose place where drugs or cosmetics are manufactured or kept
- S. 25Licences for import of drugs manufactured by one manufacturer
- S. 26Conditions of import licence
- S. 26APower of Central Government to prohibit manufacture, etc
- S. 27Grant of import licence
- S. 27APenalty for manufacture, sale, etc
- S. 28Complaints and Adverse Reactions:
- S. 28APenalty for not keeping documents, etc
- S. 28BPenalty for manufacture, etc
- S. 29Site Master File
- S. 30Prohibition of import after expiry of potency
- S. 31Confiscation
- S. 31AApplication of provisions to Government departments
- S. 32Cognizance of offence
- S. 32APower of Court to implead the manufacturer, etc
- S. 33Power of Central Government to make rules
- S. 33AChapter not to apply to Ayurvedic, Siddha or Unani drugs
- S. 33BApplication of Chapter IVA
- S. 33C12[Ayurvedic, Siddha and Unani Drugs Technical Advisory Board]
- S. 33DThe Ayurvedic, Siddha and Unani Drugs Consultative Committee
- S. 33EMisbranded drugs
- S. 33FGovernment Analysts
- S. 33GInspectors
- S. 33HApplication of provisions of sections 22, 23, 24 and 25
- S. 33JPenalty for subsequent offences
- S. 33KConfiscation
- S. 33LApplication of provisions to Government departments
- S. 33MCognizance of offences
- S. 33NPower of Central Government to make rules
- S. 33OPower to amend First Schedule
- S. 33PPower to give directions
- S. 34Offences by companies
- S. 34AOffences by Government departments
- S. 35—
- S. 36Magistrate’s power to impose enhanced penalties
- S. 36ACertain offences to be tried summarily
- S. 37Protection of action taken in good faith
- S. 38Rules to be laid before Parliament
- S. 39Documents to be supplied to the Customs Collector
- S. 40—
- S. 41—
- S. 42—
- S. 43—
- S. 44—
- S. 45Duties of Government Analysts
- S. 46Procedure on receipt of sample
- S. 47Report of result of test or analysis
- S. 48Fees
- S. 49Gentamycin Sulphate 60 In a cool place
- S. 50—
- S. 51Duties of Inspectors of premises licensed for sale
- S. 52Duties of Inspectors specially authorized to inspect the manufacture of 1[drugs or cosmetics]
- S. 53Prohibition of disclosure of information
- S. 54—
- S. 55—
- S. 56Form of intimation of purpose of taking samples
- S. 57Procedure for despatch of sample to Government Analyst
- S. 58Nystatin 36 At temperature not exceeding 5oC
- S. 59(1) The State Government shall appoint Licensing Authorities for the purpose of this Part for such areas as may be spec
- S. 60—
- S. 61(c) Biochemic tissue remedies in tablets forms, in generic names only, each in 20 gm
- S. 62Sale at more than one place
- S. 63—
- S. 64—
- S. 65Condition of licences
- S. 66Cancellation and suspension of licences
- S. 67—
- S. 67B—
- S. 67CForms of licences to sell drugs
- S. 68Manufacture on more than one set of premises
- S. 68BDelegation of Powers by the Central Licence Approving Authority
- S. 69—
- S. 70—
- S. 71—
- S. 72—
- S. 73—
- S. 74—
- S. 74AConditions for licence in Form 25-B
- S. 76—
- S. 77Strepromycin Injection
- S. 78—
- S. 79—
- S. 80—
- S. 81Procedure of Licensing Authority
- S. 82—
- S. 83Renewal
- S. 84—
- S. 85Tyrothricin 60 In a cool place
- S. 85BApplication for licence to manufacture Homoeopathic medicines
- S. 85CApplication to manufacture ‘New Homoeopathic medicines
- S. 85E—
- S. 85FDuration of licence
- S. 85GCertificate of renewal
- S. 85HConditions of licence
- S. 86Conditions relating to manufacture for examination, test or analysis
- S. 87Labelling
- S. 88Labelling of drugs supplied to other persons
- S. 89Licence
- S. 90Form of application
- S. 91Duration of licence
- S. 92Conditions of licence
- S. 93Cancellation of licences
- S. 94Exemption of certain drugs from certain provisions of this Part
- S. 95Prohibition of sale or distribution unless labelled
- S. 97Labelling of medicines
- S. 103—
- S. 108Container
- S. 110Prohibition of sale of substance after prescribed date
- S. 115Application of tests for sterility
- S. 122Substances specified in Schedule C(1)
- S. 122EDefinition of new drug
- S. 122G—
- S. 122HDuration of licence
- S. 122I—
- S. 122JReport by Inspector
- S. 122KFurther application after rejection
- S. 122LDelegation of powers by the Central Licence Approving Authority
- S. 122MProvision for appeal to the State Government by a party whose licence has not been granted or renewed
- S. 123—
- S. 128Duration of import licence
- S. 129Statement to accompany imported cosmetics
- S. 130Documents to be supplied to the Collector of Customs
- S. 131Procedure for the import of cosmetics
- S. 132—
- S. 133Import through points of entry—No cosmetic shall be imported into India except through the points of entry specified in
- S. 135Import of cosmetic containing Lead or Arsenic compound prohibited
- S. 136—
- S. 137—
- S. 138—
- S. 139—
- S. 140Procedure for the import of drugs
- S. 141Certificate of renewal
- S. 142—
- S. 143Cancellation and suspension of licence
- S. 145Use of Lead and Arsenic compounds for the purpose of colouring cosmetics prohibited
- S. 145BForm of receipt for seized cosmetics
- S. 146Prohibition of sale or distribution
- S. 148Manner of labelling
- S. 1494[Labelling of Hair dyes containing Dyes, Colours and Pigments
- S. 150Report of result of test or analysis of cosmetics
- S. 150DDuration of approval
- S. 150E—
- S. 150FInspection before grant of approval
- S. 150GReport of Inspection
- S. 150HProcedure of approving authority
- S. 150JRenewa
- S. 150K—
- S. 151Manufacture on more than one set of premises
- S. 152Licensing Authorities
- S. 153Application for licence to manufacture Ayurvedic (including Siddha) or Unani drugs
- S. 154Form of licence to manufacture Ayurvedic (including Siddha) or Unani drugs
- S. 155Certificate of renewal—The certificate of renewal of a licence in Form 25-D shall be issued in Form 26-D
- S. 156—
- S. 157Conditions for the grant or renewal of a licence in Form 25-D
- S. 158Conditions of licence
- S. 159—
- S. 160Identification of raw materials
- S. 160B—
- S. 160CDuration of approval
- S. 160DConditions of approval
- S. 160FReport of inspection
- S. 160GProcedure of approving authority
- S. 160HApplication after rejection
- S. 160JWithdrawal and suspension of approvals
- S. 1611[Labelling, packing and limit of alcohol
- S. 162—
- S. 163—
- S. 164Method of test or analysis to be employed in relation to Ayurvedic (including Siddha) or Unani drugs
- S. 165Qualifications of Government Analyst
- S. 166Duties of Government Analys
- S. 168Standards to be complied with in manufacture for sale or for distribution of Ayurvedic, Siddha and Unani Drugs
- S. 244Qualifications of Government Analyst
- S. 312—
- S. 337Packing of patent or proprietary medicine
- S. 363Duration of licence
- S. 577Duration of licence
- S. 614—
- S. 776—
- S. 871Conditions for the grant or renewal of a licence in Form 25 9[or Form 25-F]
- S. 1111Standards
- S. 1124BStandards for patent or proprietary medicines
- S. 1127List of colours permitted to be used in drugs
- S. 1141ACertificate of renewal of a loan licence—The certificate of renewal of a licence in Form 32-A shall be issued in Form 3
- S. 1142BConditions of licence in Form 32-A
- S. 1167Qualifications of Inspector
- S. 1940Date of issue: ………
- S. 1945We operate a pharmacy on the premises, situated at
- S. 1996—
- S. 2107Name of substance
- S. 2109Labelling
- S. 2112Tests for strength and quality
- S. 2121A—
- S. 2124—
- S. 2139BForm of loan 3[licence to manufacture cosmetics for sale or for distribution]
- S. 2145AForm of intimation for purpose of taking samples of cosmetics
- S. 3124AStandards for veterinary drugs
- S. 4125Standards for substances (other than food) intended to affect the structure or any function of human body—contraceptive
- S. 6126—