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U.S. Department of Health and Human Services

CFR - Code of Federal Regulations Title 21

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The information on this page is current as of Oct 01, 2021.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER D - DRUGS FOR HUMAN USE
 
PART 332ANTIFLATULENT PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
 

Subpart A - General Provisions
   § 332.1 - Scope.
   § 332.3 - Definitions.

Subpart B - Active Ingredients
   § 332.10 - Antiflatulent active ingredients.
   § 332.15 - Combination with non-antiflatulent active ingredients.

Subpart C - Labeling
   § 332.30 - Labeling of antiflatulent drug products.
   § 332.31 - Professional labeling.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 39 FR 19877, June 4, 1974, unless otherwise noted.

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