Title 21

PART 358

Part 358 - Miscellaneous External Drug Products For Over-the-counter Human Use

PART 358 - MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE Authority:21 U.S.C. 321, 351, 352, 353, 355, 360, 371. Source:55 FR 33255, Aug. 14, 1990, unless otherwise noted.

21:5.0.1.1.30.1SUBPART A
Subpart A [Reserved]
21:5.0.1.1.30.2SUBPART B
Subpart B - Wart Remover Drug Products
21:5.0.1.1.30.2.1.1SECTION 358.101
   358.101 Scope.
21:5.0.1.1.30.2.1.2SECTION 358.103
   358.103 Definitions.
21:5.0.1.1.30.2.1.3SECTION 358.110
   358.110 Wart remover active ingredients.
21:5.0.1.1.30.2.1.4SECTION 358.150
   358.150 Labeling of wart remover drug products.
21:5.0.1.1.30.3SUBPART C
Subpart C [Reserved]
21:5.0.1.1.30.4SUBPART D
Subpart D - Ingrown Toenail Relief Drug Products
21:5.0.1.1.30.4.1.1SECTION 358.301
   358.301 Scope.
21:5.0.1.1.30.4.1.2SECTION 358.303
   358.303 Definitions.
21:5.0.1.1.30.4.1.3SECTION 358.310
   358.310 Ingrown toenail relief active ingredient.
21:5.0.1.1.30.4.1.4SECTION 358.350
   358.350 Labeling of ingrown toenail relief drug products.
21:5.0.1.1.30.5SUBPART E
Subpart E [Reserved]
21:5.0.1.1.30.6SUBPART F
Subpart F - Corn and Callus Remover Drug Products
21:5.0.1.1.30.6.1.1SECTION 358.501
   358.501 Scope.
21:5.0.1.1.30.6.1.2SECTION 358.503
   358.503 Definitions.
21:5.0.1.1.30.6.1.3SECTION 358.510
   358.510 Corn and callus remover active ingredients.
21:5.0.1.1.30.6.1.4SECTION 358.550
   358.550 Labeling of corn and callus remover drug products.
21:5.0.1.1.30.7SUBPART G
Subpart G - Pediculicide Drug Products
21:5.0.1.1.30.7.1.1SECTION 358.601
   358.601 Scope.
21:5.0.1.1.30.7.1.2SECTION 358.603
   358.603 Definition.
21:5.0.1.1.30.7.1.3SECTION 358.610
   358.610 Pediculicide active ingredients.
21:5.0.1.1.30.7.1.4SECTION 358.650
   358.650 Labeling of pediculicide drug products.
21:5.0.1.1.30.8SUBPART H
Subpart H - Drug Products for the Control of Dandruff, Seborrheic Dermatitis, and Psoriasis
21:5.0.1.1.30.8.1.1SECTION 358.701
   358.701 Scope.
21:5.0.1.1.30.8.1.2SECTION 358.703
   358.703 Definitions.
21:5.0.1.1.30.8.1.3SECTION 358.710
   358.710 Active ingredients for the control of dandruff, seborrheic dermatitis, or psoriasis.
21:5.0.1.1.30.8.1.4SECTION 358.720
   358.720 Permitted combinations of active ingredients.
21:5.0.1.1.30.8.1.5SECTION 358.750
   358.750 Labeling of drug products for the control of dandruff, seborrheic dermatitis, or psoriasis.
21:5.0.1.1.30.8.1.6SECTION 358.760
   358.760 Labeling of permitted combinations of active ingredients for the control of dandruff.