Home NDC 52063-709 ACNE FORTE Acne Treatment Cream
Product NDC 52063-709
11-digit product format 520630709
Labeler code 52063
Product ID 52063-709_09d72888-7c83-700d-e063-6394a90a701b
Type HUMAN OTC DRUG
Nonproprietary name BENZOYL PEROXIDE
Dosage form CREAM
Route TOPICAL
Labeler GSCM Ventures Inc. DBA Revitol
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-01-10
Substance BENZOYL PEROXIDE
Active strength 50 mg/mL
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 ACNE FORTE Acne Treatment Cream
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength BENZOYL PEROXIDE 50 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 308693 Internal RxNorm 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 52063-709-00 ACNE FORTE Acne Treatment Cream 59 mL in 1 JAR CREAM 59 2 52063-709-00 ACNE FORTE Acne Treatment Cream 1 in 1 BOX CREAM 1 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 52063-709 ACNE FORTE ACNE TREATMENT CREAM (BENZOYL PEROXIDE) CREAM [GSCM VENTURES INC. DBA REVITOL] 2 Current NDC, Legacy NDC, 2 package rows 20231111_c29ed6c1-b8ad-4131-a94c-379f16ab2ee5.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 7 of 56 · 1,101 matching rows.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 52063-709-00 52063070900 1 JAR in 1 BOX (52063-709-00) / 59 mL in 1 JAR 1 jar 2022-01-10 0000-00-00 No No Current