Home NDC 46122-525 Benzethonium chloride Plus Dyclonine hydrochloride
Product NDC 46122-525
11-digit product format 461220525
Labeler code 46122
Product ID 46122-525_4094cd51-7445-fa2b-e063-6294a90ab4e8
Type HUMAN OTC DRUG
Nonproprietary name Liquid Bandage
Dosage form LIQUID
Route TOPICAL
Labeler AmerisourceBergen Drug Corporation
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2017-12-21
Substance BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength .2; .75 mg/9mL; mg/9mL
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 Benzethonium chloride Plus Dyclonine hydrochloride
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE .2 mg/9mL DYCLONINE HYDROCHLORIDE .75 mg/9mL
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 46122-525-23 Benzethonium chloride Plus Dyclonine hydrochloride 9 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 9 8
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 46122-525 BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [AMERISOURCEBERGEN DRUG CORPORATION] 7 Current NDC, Legacy NDC, 1 package rows 20241123_5c82c4db-258e-4647-aec9-1c4520e0468a.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 85 of 114 · 2,270 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 46122-525-23 46122052523 9 mL in 1 BOTTLE, WITH APPLICATOR (46122-525-23) 9 ml 2017-12-21 0000-00-00 No No Current