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[A1]

 

Electronic Code of Federal Regulations

e-CFR data is current as of April 2, 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.

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