 |
Code of Federal Regulations (Last Updated: November 8, 2024) |
 |
Title 21 - Food and Drugs |
|
|
Chapter I - Food and Drug Administration, Department of Health and Human Services |
|
|
SubChapter D - Drugs for Human Use |
|
|
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. |