1[(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 2
[the Second Schedule], and
(b) in relation to a cosmetic, that the cosmetic complies with such standard as may be prescribed.
(2) The 3 [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 2 [the Second Schedule] for the purposes of this Chapter, and thereupon 2 [the Second Schedule] shall be deemed to be amended accordingly.
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1. Subs. by Act 21 of 1962, s. 12, for sub-section (1) (w.e.f. 27-7-1964).
2. Subs. by Act 13 of 1964, s. 11, for "the Schedule" (w.e.f. 15-9-1964).
3. Subs. by Act 11 of 1955, s. 8, for "State Government"
Section 16 Standards of quality
Section 17C Misbranded cosmetics
Section 17D Spurious cosmetics
Section 17E Adulterated cosmetics
Section 18 Prohibition of manufacture and sale of certain drugs and cosmetics
Section 18A Disclosure of the name of the manufacturer, etc
Section 18B Maintenance of records and furnishing of information
Section 20 Government Analysts
Section 22 Powers of Inspectors
Section 23 Procedure of Inspectors
Section 24 Persons bound to disclose place where drugs or cosmetics are manufactured or kept
Section 25 Reports of Government Analysts
Section 26 Purchaser of drug or cosmetic enabled to obtain test or analysis
Section 27 Penalty for manufacture, sale, etc., of drugs in contravention of this Chapter
Section 27A Penalty for manufacture, sale, etc., of cosmetics in contravention of this Chapter
Section 28 Penalty for non-disclosure of the name of the manufacturer, etc
Section 28A Penalty for not keeping documents, etc., and for non-disclosure of information
Section 28B Penalty for manufacture, etc., of drugs or cosmetics in contravention of section 26A
Section 29 Penalty for use of Government Analyst's report for advertising