Home NDC 68016-615 Benzethonium chloride Plus Dyclonine hydrochloride
Product NDC 68016-615
11-digit product format 680160615
Labeler code 68016
Product ID 68016-615_4aa79801-8b17-6930-e063-6394a90ae687
Type HUMAN OTC DRUG
Nonproprietary name Liquid Bandage
Dosage form LIQUID
Route TOPICAL
Labeler Chain Drug Consortium, LLC
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2005-12-07
Marketing end 2027-04-30
Substance BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength .2; .75 mg/9mL; mg/9mL
NDC exclude flag No
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 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 68016-615-00 Benzethonium chloride Plus Dyclonine hydrochloride 9 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 9 14
DailyMed Socrata Ingredients# Ingredient, Type, UNII table Ingredient Type UNII DailyMed label SPL version Uploaded BENZETHONIUM CHLORIDE ACTIVE INGREDIENT PH41D05744 BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 DYCLONINE HYDROCHLORIDE ACTIVE INGREDIENT ZEC193879Q BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 BENZETHONIUM ACTIVE MOIETY 1VU15B70BP BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 DYCLONINE ACTIVE MOIETY 078A24Q30O BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 ACETONE INACTIVE INGREDIENT 1364PS73AF BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 ALCOHOL INACTIVE INGREDIENT 3K9958V90M BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 AMYL ACETATE INACTIVE INGREDIENT 92Q24NH7AS BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 CASTOR OIL INACTIVE INGREDIENT D5340Y2I9G BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 ETHYL ACETATE INACTIVE INGREDIENT 76845O8NMZ BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2 PYROXYLIN INACTIVE INGREDIENT KYR8BR2X6O BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 68016-615 BENZETHONIUM CHLORIDE PLUS DYCLONINE HYDROCHLORIDE (LIQUID BANDAGE) LIQUID [CHAIN DRUG CONSORTIUM, LLC] 11 Current NDC, Legacy NDC, 1 package rows 20241213_d7154398-4f52-434a-b51b-b7829ccebf3b.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 44 of 115 · 2,286 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 68016-615-00 68016061500 9 mL in 1 BOTTLE, WITH APPLICATOR (68016-615-00) 9 ml 2005-12-07 2027-04-30 No No Current