Home NDC 53228-231-01 finipil 4 men only
Product NDC 53228-231
Requested package NDC 53228-231-01
11-digit product format 532280231
Labeler code 53228
Product ID 53228-231_463269d3-0c65-62e1-e063-6394a90a1c6b
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium Chloride
Dosage form LIQUID
Route TOPICAL
Labeler Equibal, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2014-08-01
Substance BENZETHONIUM CHLORIDE
Active strength 200 mg/1000mg
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 finipil 4 men only
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE 200 mg/1000mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination PH41D05744 Internal UNII lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 53228-231-01 finipil 4 men only 236000 mg in 1 BOTTLE, PUMP LIQUID 236000 12 53228-231-02 finipil 4 men only 118000 mg in 1 BOTTLE, PUMP LIQUID 118000 12
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 53228-231-01 53228023101 236000 mg in 1 BOTTLE, PUMP (53228-231-01) 236000 mg 2014-08-01 0000-00-00 No No Current