Clinical Trials

Find trials by condition, location & phase

Drug Monographs

Browse drug monographs and information

Explore organizations and their profiles

Latest updates on trials and healthcare

Approved products by global authorities

AI-Powered Research

Discover powerful insights with advanced AI analysis tools for clinical trials.

Premium Access

Get unlimited access to our comprehensive pharmaceutical database and analytics.

FDA Approval

Benzethonium chloride and Dyclonine hydrochloride

CompanyChain Drug Marketing Association (DUNS: 011920774)

Effective Date

May 1, 2025

Labeling Type

HUMAN OTC DRUG LABEL

Active Ingredients

Benzethonium Chloride(2 mg in 1 mL)

Dyclonine Hydrochloride(7.5 mg in 1 mL)

Products (1)

Benzethonium chloride and Dyclonine hydrochloride

NDC Product Code

83324-232

Application Number

M003

Marketing Category

OTC Monograph Drug (C200263)

Route of Administration

TOPICAL

Effective Date

May 1, 2025

Ingredients

ACETONEInactive

Code: 1364PS73AFClass: IACT

AMYL ACETATEInactive

Code: 92Q24NH7ASClass: IACT

CASTOR OILInactive

Code: D5340Y2I9GClass: IACT

ETHYL ACETATEInactive

Code: 76845O8NMZClass: IACT

PYROXYLINInactive

Code: KYR8BR2X6OClass: IACT

ALCOHOLInactive

Code: 3K9958V90MClass: IACT

Benzethonium ChlorideActive

Code: PH41D05744Class: ACTIBQuantity: 2 mg in 1 mL

Dyclonine HydrochlorideActive

Code: ZEC193879QClass: ACTIBQuantity: 7.5 mg in 1 mL

© Copyright 2025. All Rights Reserved by MedPath

Home Terms & Conditions Privacy Policy