Home NDC 0363-1364 Walgreens Acne Foaming Cleanser
Product NDC 0363-1364
11-digit product format 003631364
Labeler code 0363
Product ID 0363-1364_549fea8d-70bb-ad68-e063-6294a90a48a8
Type HUMAN OTC DRUG
Nonproprietary name BENZOYL PEROXIDE
Dosage form CREAM
Route TOPICAL
Labeler WALGREEN COMPANY
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-01
Substance BENZOYL PEROXIDE
Active strength 40 mg/mL
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 Walgreens Acne Foaming Cleanser
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOYL PEROXIDE 40 mg/mL
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 1539352 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 42 of 54 · 1,079 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 0363-1364-23 00363136423 150 mL in 1 TUBE (0363-1364-23) 150 ml 2026-09-01 No No Current