Home NDC 82442-019 Benzethonium chloride and Dyclonine hydrochloride
Product NDC 82442-019
11-digit product format 824420019
Labeler code 82442
Product ID 82442-019_54d94a26-03f6-ce49-e063-6294a90a7e53
Type HUMAN OTC DRUG
Nonproprietary name Liquid Bandage
Dosage form LIQUID
Route TOPICAL
Labeler Target Corporation
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-04-09
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 82442-019-01 Benzethonium chloride and Dyclonine hydrochloride 29.6 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 29.6 3 82442-019-01 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 82442-019 BENZETHONIUM CHLORIDE AND DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [TARGET CORPORATION] 2 Current NDC, 2 package rows 20250417_326daa64-165a-cea6-e063-6294a90afbab.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 9 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 82442-019-01 82442001901 1 BOTTLE, WITH APPLICATOR in 1 CARTON (82442-019-01) / 29.6 mL in 1 BOTTLE, WITH APPLICATOR 2025-04-09 No No Current