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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 April 1 2018.

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 347SKIN PROTECTANT DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
 

Subpart A--General Provisions
   § 347.1 - Scope.
   § 347.3 - Definitions.

Subpart B--Active Ingredients
   § 347.10 - Skin protectant active ingredients.
   § 347.12 - Astringent active ingredients.
   § 347.20 - Permitted combinations of active ingredients.

Subpart C--Labeling
   § 347.50 - Labeling of skin protectant drug products.
   § 347.52 - Labeling of astringent drug products.
   § 347.60 - Labeling of permitted combinations of active ingredients.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 58 FR 54462, Oct. 21, 1993, unless otherwise noted.

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