e-CFR banner

Home
gpo.gov
govinfo.gov

e-CFR Navigation Aids

Browse

Simple Search

Advanced Search

 — Boolean

 — Proximity

 

Search History

Search Tips

Corrections

Latest Updates

User Info

FAQs

Agency List

Incorporation By Reference

eCFR logo

Related Resources

The Code of Federal Regulations (CFR) annual edition is the codification of the general and permanent rules published in the Federal Register by the departments and agencies of the Federal Government produced by the Office of the Federal Register (OFR) and the Government Publishing Office.

Download the Code of Federal Regulations in XML.

Download the Electronic Code of Federal Regulations in XML.

Monthly Title and Part user viewing data for the e-CFR is available for download in CSV format.

Parallel Table of Authorities and Rules for the Code of Federal Regulations and the United States Code
Text | PDF

Find, review, and submit comments on Federal rules that are open for comment and published in the Federal Register using Regulations.gov.

Purchase individual CFR titles from the U.S. Government Online Bookstore.

Find issues of the CFR (including issues prior to 1996) at a local Federal depository library.

[A1]

 

Electronic Code of Federal Regulations

e-CFR data is current as of February 13, 2020

Title 21 → Chapter I → Subchapter D → Part 358

TITLE 21—Food and Drugs

CHAPTER I—FOOD AND DRUG ADMINISTRATION, DEPARTMENT OF HEALTH AND HUMAN SERVICES (CONTINUED)

SUBCHAPTER D—DRUGS FOR HUMAN USE

PART 358—MISCELLANEOUS EXTERNAL DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE

rule

Subpart A—[RESERVED]

rule

Subpart B—WART REMOVER DRUG PRODUCTS

§358.101
Scope.
§358.103
Definitions.
§358.110
Wart remover active ingredients.
§358.150
Labeling of wart remover drug products.
rule

Subpart C—[RESERVED]

rule

Subpart D—INGROWN TOENAIL RELIEF DRUG PRODUCTS

§358.301
Scope.
§358.303
Definitions.
§358.310
Ingrown toenail relief active ingredient.
§358.350
Labeling of ingrown toenail relief drug products.
rule

Subpart E—[RESERVED]

rule

Subpart F—CORN AND CALLUS REMOVER 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.
rule

Subpart G—PEDICULICIDE DRUG PRODUCTS

§358.601
Scope.
§358.603
Definition.
§358.610
Pediculicide active ingredients.
§358.650
Labeling of pediculicide drug products.
rule

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.

Need assistance?