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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 Aug 30, 2024.

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 350ANTIPERSPIRANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
 

Subpart A - General Provisions
   § 350.1 - Scope.
   § 350.3 - Definition.

Subpart B - Active Ingredients
   § 350.10 - Antiperspirant active ingredients.

Subpart C - Labeling
   § 350.50 - Labeling of antiperspirant drug products.

Subpart D - Guidelines for Effectiveness Testing
   § 350.60 - Guidelines for effectiveness testing of antiperspirant drug products.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 68 FR 34291, June 9, 2003, unless otherwise noted.

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