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Code of Federal Regulations › Title 21 › Part 358

Part 358 — Miscellaneous External Drug Products for Over-the-Counter Human Use

Current through Sep 8, 2026

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.

Source: 55 FR 33255, Aug. 14, 1990, unless otherwise noted.

Sections

  • § 358.101 Scope.
  • § 358.103 Definitions.
  • § 358.110 Wart remover active ingredients.
  • § 358.150 Labeling of wart remover drug products.
  • § 358.301 Scope.
  • § 358.303 Definitions.
  • § 358.310 Ingrown toenail relief active ingredient.
  • § 358.350 Labeling of ingrown toenail relief 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.
  • § 358.601 Scope.
  • § 358.603 Definition.
  • § 358.610 Pediculicide active ingredients.
  • § 358.650 Labeling of pediculicide drug products.
  • § 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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