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Code of Federal Regulations (Last Updated: July 5, 2024) |
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Title 21 - Food and Drugs |
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Chapter I - Food and Drug Administration, Department of Health and Human Services |
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SubChapter D - Drugs for Human Use |
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Part 358 - Miscellaneous External Drug Products for over-the-Counter Human Use |
Subpart A - XXX |
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 - XXX |
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 - XXX |
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. |