Home NDC 87770-025 Dr Marvel ANTI DANDRUFF SCALP SERUM
Product NDC 87770-025
11-digit product format 877700025
Labeler code 87770
Product ID 87770-025_5aaede65-c08d-c4ea-e063-6294a90a947b
Type HUMAN OTC DRUG
Nonproprietary name Selenium Sulfide Salicylic Acid
Dosage form SOLUTION
Route TOPICAL
Labeler Guangzhou Liyan Cosmetics Technology Co., Ltd.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-05
Substance SALICYLIC ACID; SELENIUM SULFIDE
Active strength 2; 2 mg/100mg; mg/100mg
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 Dr Marvel ANTI DANDRUFF SCALP SERUM
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 2 mg/100mg SELENIUM SULFIDE 2 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup Z69D9E381Q Internal UNII 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 16 of 31 · 615 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87770-025-01 87770002501 100 mg in 1 BOX (87770-025-01) 100 mg 2026-09-05 No No Current