Home NDC 56104-502 Liquid Bandage
Product NDC 56104-502
11-digit product format 561040502
Labeler code 56104
Product ID 56104-502_4094375b-31ea-3c3a-e063-6294a90ad8f6
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium chloride Plus Dyclonine hydrochloride
Dosage form LIQUID
Route TOPICAL
Labeler Premier Brands of America Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2023-09-11
Substance BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength 2; 7.5 mg/mL; mg/mL
NDC exclude flag No
Listing certified through 2026-12-31
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 Liquid Bandage
Listing expiration 2026-12-31 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 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 56104-502-00 Liquid Bandage 29.6 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 29.6 5 56104-502-00 Liquid Bandage 1 in 1 CARTON LIQUID 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56104-502 LIQUID BANDAGE (BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE) LIQUID [PREMIER BRANDS OF AMERICA INC.] 4 Current NDC, 2 package rows 20241016_051b68f9-5d6c-3cd7-e063-6394a90aeb35.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 99 of 114 · 2,275 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Marketing start Sample Exclude flag Status 56104-502-00 56104050200 1 BOTTLE, WITH APPLICATOR in 1 CARTON (56104-502-00) / 29.6 mL in 1 BOTTLE, WITH APPLICATOR 2023-09-11 No No Current