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U.S. Department of Health and Human Services

CFR - Code of Federal Regulations Title 21

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The information on this page is current as of Oct 01, 2021.

For the most up-to-date version of CFR Title 21, go to the Electronic Code of Federal Regulations (eCFR).

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TITLE 21--FOOD AND DRUGS
CHAPTER I--FOOD AND DRUG ADMINISTRATION
DEPARTMENT OF HEALTH AND HUMAN SERVICES
SUBCHAPTER D - DRUGS FOR HUMAN USE
 
PART 341COLD, COUGH, ALLERGY, BRONCHODILATOR, AND ANTIASTHMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE
 

Subpart A - General Provisions
   § 341.1 - Scope.
   § 341.3 - Definitions.

Subpart B - Active Ingredients
   § 341.12 - Antihistamine active ingredients.
   § 341.14 - Antitussive active ingredients.
   § 341.16 - Bronchodilator active ingredients.
   § 341.18 - Expectorant active ingredient.
   § 341.20 - Nasal decongestant active ingredients.
   § 341.40 - Permitted combinations of active ingredients.

Subpart C - Labeling
   § 341.70 - Labeling of OTC drug products containing ingredients that are used for treating concurrent symptoms (in either a single-ingredient or combination drug product).
   § 341.72 - Labeling of antihistamine drug products.
   § 341.74 - Labeling of antitussive drug products.
   § 341.76 - Labeling of bronchodilator drug products.
   § 341.78 - Labeling of expectorant drug products.
   § 341.80 - Labeling of nasal decongestant drug products.
   § 341.85 - Labeling of permitted combinations of active ingredients.
   § 341.90 - Professional labeling.

Authority: 21 U.S.C. 321, 351, 352, 353, 355, 360, 371.

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