Home NDC 56104-246 Premier Solutions Liquid Bandage
Product NDC 56104-246
11-digit product format 561040246
Labeler code 56104
Product ID 56104-246_4096871d-bc42-b86a-e063-6294a90afe8b
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium chloride Dyclonine hydrochloride
Dosage form LIQUID
Route TOPICAL
Labeler Premier Brands of America, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-06-16
Substance BENZETHONIUM CHLORIDE; DYCLONINE HYDROCHLORIDE
Active strength .2; .75 mg/10mL; mg/10mL
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 Premier Solutions Liquid Bandage
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE .2 mg/10mL DYCLONINE HYDROCHLORIDE .75 mg/10mL
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 56104-246-01 Premier Solutions Liquid Bandage 10 mL in 1 BOTTLE, WITH APPLICATOR LIQUID 10 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 56104-246 PREMIER SOLUTIONS LIQUID BANDAGE (BENZETHONIUM CHLORIDE DYCLONINE HYDROCHLORIDE) LIQUID [PREMIER BRANDS OF AMERICA, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20241016_e196d4c2-a93e-a03c-e053-2995a90a3ea3.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 27 of 117 · 2,333 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 56104-246-01 56104024601 10 mL in 1 BOTTLE, WITH APPLICATOR (56104-246-01) 10 ml 2022-06-16 0000-00-00 No No Current