Home NDC 53228-232-01 Made for Men
Product NDC 53228-232
Requested package NDC 53228-232-01
11-digit product format 532280232
Labeler code 53228
Product ID 53228-232_46333491-0c21-46c9-e063-6294a90a1159
Type HUMAN OTC DRUG
Nonproprietary name Benzethonium Chloride
Dosage form LOTION
Route TOPICAL
Labeler Equibal, Inc.
Application M003
Marketing category OTC MONOGRAPH DRUG
Marketing start 2016-04-01
Substance BENZETHONIUM CHLORIDE
Active strength .2 mg/mg
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 Made for Men
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZETHONIUM CHLORIDE .2 mg/mg
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 53228-232-01 Made for Men 236000 mg in 1 BOTTLE, PUMP LOTION 236000 8 53228-232-02 Made for Men 118000 mg in 1 BOTTLE, PUMP LOTION 118000 8
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 100 of 114 · 2,277 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 53228-232-01 53228023201 236000 mg in 1 BOTTLE, PUMP (53228-232-01) 236000 mg 2016-04-01 0000-00-00 No No Current