Home NDC 84509-114 Acne Relief
Product NDC 84509-114
11-digit product format 845090114
Labeler code 84509
Product ID 84509-114_59db0143-de58-59d2-e063-6294a90a32a8
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID,NIACINAMIDE,PANTHENOL.
Dosage form CREAM
Route TOPICAL
Labeler Guangzhou Senmai Biotechnology Co.,Ltd.
Application M016
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-08-25
Substance SALICYLIC ACID; NIACINAMIDE; PANTHENOL; AZELAMIDE MEA; ALLANTOIN
Active strength 500; 500; 250; 210; 100 mg/50mL; mg/50mL; mg/50mL; mg/50mL; mg/50mL
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 Acne Relief
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 500 mg/50mL NIACINAMIDE 500 mg/50mL PANTHENOL 250 mg/50mL AZELAMIDE MEA 210 mg/50mL ALLANTOIN 100 mg/50mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 5 matching rows.
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 39 of 68 · 1,357 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 84509-114-01 84509011401 50 mL in 1 BOTTLE (84509-114-01) 50 ml 2026-08-25 No No Current