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Code of Federal Regulations (Last Updated: November 8, 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 |
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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. |