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

 

Electronic Code of Federal Regulations

e-CFR data is current as of June 4, 2020

Title 21Chapter ISubchapter DPart 341


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 341—COLD, COUGH, ALLERGY, BRONCHODILATOR, AND ANTIASTHMATIC DRUG PRODUCTS FOR OVER-THE-COUNTER HUMAN USE

rule

Subpart A—GENERAL PROVISIONS

§341.1
Scope.
§341.3
Definitions.
rule

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.
rule

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.

Need assistance?