Home NDC 83324-232 Benzethonium chloride and Dyclonine hydrochloride
Product NDC 83324-232
11-digit product format 833240232
Labeler code 83324
Product ID 83324-232_53d7a1c1-cad4-780c-e063-6394a90aa094
Type HUMAN OTC DRUG
Nonproprietary name Liquid Bandage
Dosage form LIQUID
Route TOPICAL
Labeler Chain Drug Marketing Association
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-17
Substance BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength 2; 7.5 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.
Additional Listing Data#
Finished product Yes
Brand name base Benzethonium chloride and Dyclonine hydrochloride
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE 2 mg/mL DYCLONINE HYDROCHLORIDE 7.5 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PH41D05744 Internal UNII lookup ZEC193879Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1048366 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83324-232-03 Benzethonium chloride and Dyclonine hydrochloride 9 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 9 3 83324-232-03 Benzethonium chloride and Dyclonine hydrochloride 1 in 1 CARTON LIQUID 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 83324-232 BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG MARKETING ASSOCIATION] 1 Current NDC, 2 package rows 20250504_34062b23-52aa-99ae-e063-6294a90ae73f.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 100 of 115 · 2,286 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 83324-232-03 83324023203 1 BOTTLE, WITH APPLICATOR in 1 CARTON (83324-232-03) / 9 mL in 1 BOTTLE, WITH APPLICATOR 2025-04-25 No No Current