Home NDC 51326-176 RFA BPO Acne Treatment
Product NDC 51326-176
11-digit product format 513260176
Labeler code 51326
Product ID 51326-176_62739ef1-542e-449d-aaad-c98403d7f895
Type HUMAN OTC DRUG
Nonproprietary name Benzoyl Peroxide
Dosage form LIQUID
Route TOPICAL
Labeler Topiderm, Inc.
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-12-21
Substance BENZOYL PEROXIDE
Active strength 25 mg/g
NDC exclude flag No
Listing certified through 2027-12-31
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 RFA BPO Acne Treatment
Brand name suffix 2.5%
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOYL PEROXIDE 25 mg/g
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination W9WZN9A0GM Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 200009 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 8 of 55 · 1,088 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 51326-176-01 51326017601 1 BOTTLE in 1 BOX (51326-176-01) / 57 g in 1 BOTTLE 1 bottle 2024-12-21 No No Current