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  1. LII
  2. Electronic Code of Federal Regulations (e-CFR)
  3. Title 21 - Food and Drugs
  4. CHAPTER I - FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES
  5. SUBCHAPTER D - DRUGS FOR HUMAN USE
  6. PART 358 - MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
  7. Subpart H - Drug Products for the Control of Dandruff, Seborrheic Dermatitis, and Psoriasis

21 CFR Subpart H - Drug Products for the Control of Dandruff, Seborrheic Dermatitis, and Psoriasis

  • CFR
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  1. § 358.701 Scope.
  2. § 358.703 Definitions.
  3. § 358.710 Active ingredients for the control of dandruff, seborrheic dermatitis, or psoriasis.
  4. § 358.720 Permitted combinations of active ingredients.
  5. § 358.750 Labeling of drug products for the control of dandruff, seborrheic dermatitis, or psoriasis.
  6. § 358.760 Labeling of permitted combinations of active ingredients for the control of dandruff.
Source:
56 FR 63568, Dec. 4, 1991, unless otherwise noted.

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