Site Feedback

Title 21

Displaying title 21, up to date as of 9/23/2021. Title 21 was last amended 9/21/2021.
eCFR Content

The Code of Federal Regulations (CFR) is the official legal print publication containing the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government. The Electronic Code of Federal Regulations (eCFR) is a continuously updated online version of the CFR. It is not an official legal edition of the CFR.

Learn more about the eCFR, its status, and the editorial process.

Title 21 Food and Drugs Part / Section
Chapter I Food and Drug Administration, Department of Health and Human Services 1 – 1299
Subchapter D Drugs for Human Use 300 – 499
Part 358 Miscellaneous External Drug Products for Over-the-Counter Human Use 358.101 – 358.760
Subpart A [Reserved]
Subpart B Wart Remover Drug Products 358.101 – 358.150
§ 358.101 Scope.
§ 358.103 Definitions.
§ 358.110 Wart remover active ingredients.
§ 358.150 Labeling of wart remover drug products.
Subpart C [Reserved]
Subpart D Ingrown Toenail Relief Drug Products 358.301 – 358.350
§ 358.301 Scope.
§ 358.303 Definitions.
§ 358.310 Ingrown toenail relief active ingredient.
§ 358.350 Labeling of ingrown toenail relief drug products.
Subpart E [Reserved]
Subpart F Corn and Callus Remover Drug Products 358.501 – 358.550
§ 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 – 358.650
§ 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 – 358.760