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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.


Parallel Table of Authorities and Rules for the Code of Federal Regulations and the United States Code
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Electronic Code of Federal Regulations

Electronic Code of Federal Regulations

e-CFR data is current as of July 30, 2015

Title 21Chapter ISubchapter DPart 343


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 343—INTERNAL ANALGESIC, ANTIPYRETIC, AND ANTIRHEUMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE

rule

Subpart A—GENERAL PROVISIONS

§343.1
Scope.
§343.3
Definitions.
rule

Subpart B—ACTIVE INGREDIENTS

§343.10
[Reserved]
§343.12
Cardiovascular active ingredients.
§343.13
Rheumatologic active ingredients.
§343.20
[Reserved]
§343.22
Permitted combinations of active ingredients for cardiovascular-rheumatologic use.
rule

Subpart C—LABELING

§§343.50-343.60
[Reserved]
§343.80
Professional labeling.
rule

Subpart D—TESTING PROCEDURES

§343.90
Dissolution and drug release testing.

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