21 CFR Part 358
PART 358—MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
- PART 358—MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
- Chapter I—Food and Drug Administration, Department of Health and Human Services › Subchapter D—Drugs for 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.
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