Home NDC 49967-172 CeraVe Developed with Dermatologists Acne Control Acne Treatment
Product NDC 49967-172
11-digit product format 499670172
Labeler code 49967
Product ID 49967-172_dc3ff666-19b7-4146-8eed-e28b7689274d
Type HUMAN OTC DRUG
Nonproprietary name Salicylic Acid
Dosage form GEL
Route TOPICAL
Labeler L'Oreal USA Products Inc
Application M006
Marketing category OTC MONOGRAPH DRUG
Marketing start 2021-05-18
Substance SALICYLIC ACID
Active strength 20 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 CeraVe Developed with Dermatologists Acne Control Acne Treatment
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 20 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 346298 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 49967-172-01 CeraVe Developed with Dermatologists Acne Control Acne Treatment 1 in 1 CARTON GEL 1 2 49967-172-01 CeraVe Developed with Dermatologists Acne Control Acne Treatment 40 mL in 1 TUBE GEL 40 2
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 49967-172 CERAVE DEVELOPED WITH DERMATOLOGISTS ACNE CONTROL ACNE TREATMENT (SALICYLIC ACID) GEL [L'OREAL USA PRODUCTS INC] 2 Current NDC, Legacy NDC, 2 package rows 20240101_2532352e-eabc-4565-9437-b8801db6937a.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 14 of 55 · 1,088 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 49967-172-01 49967017201 1 TUBE in 1 CARTON (49967-172-01) / 40 mL in 1 TUBE 1 tube 2021-05-18 0000-00-00 No No Current