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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 2017.

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 358MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
 

Subpart A [Reserved]

Subpart B--Wart Remover Drug Products
   § 358.101 - Scope.
   § 358.103 - Definitions.
   § 358.110 - Wart remover active ingredients.
   § 358.150 - Labeling of wart remover drug products.

Subpart C [Reserved]

Subpart D--Ingrown Toenail Relief Drug Products
   § 358.301 - Scope.
   § 358.303 - Definitions.
   § 358.310 - Ingrown toenail relief active ingredient.
   § 358.350 - Labeling of ingrown toenail relief drug products.

Subpart E [Reserved]

Subpart F--Corn and Callus Remover Drug Products
   § 358.501 - Scope.
   § 358.503 - Definitions.
   § 358.510 - Corn and callus remover active ingredients.
   § 358.550 - Labeling of corn and callus remover drug products.

Subpart G--Pediculicide Drug Products
   § 358.601 - Scope.
   § 358.603 - Definition.
   § 358.610 - Pediculicide active ingredients.
   § 358.650 - Labeling of pediculicide drug products.

Subpart H--Drug Products for the Control of Dandruff, Seborrheic Dermatitis, and Psoriasis
   § 358.701 - Scope.
   § 358.703 - Definitions.
   § 358.710 - Active ingredients for the control of dandruff, seborrheic dermatitis, or psoriasis.
   § 358.720 - Permitted combinations of active ingredients.
   § 358.750 - Labeling of drug products for the control of dandruff, seborrheic dermatitis, or psoriasis.
   § 358.760 - Labeling of permitted combinations of active ingredients for the control of dandruff.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.
Source: 55 FR 33255, Aug. 14, 1990, unless otherwise noted.

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