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Electronic Code of Federal Regulations

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e-CFR Data is current as of November 26, 2014

Title 21Chapter ISubchapter DPart 352


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 352—SUNSCREEN DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE [STAYED INDEFINITELY]

rule

Subpart A—GENERAL PROVISIONS

§352.1
Scope.
§352.3
Definitions.
rule

Subpart B—ACTIVE INGREDIENTS

§352.10
Sunscreen active ingredients.
§352.20
Permitted combinations of active ingredients.
rule

Subpart C—LABELING

§352.50
Principal display panel of all sunscreen drug products.
§352.52
Labeling of sunscreen drug products.
§352.60
Labeling of permitted combinations of active ingredients.
rule

Subpart D—TESTING PROCEDURES

§352.70
Standard sunscreen.
§352.71
Light source (solar simulator).
§352.72
General testing procedures.
§352.73
Determination of SPF value.
§352.76
Determination if a product is water resistant or very water resistant.
§352.77
Test modifications.


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