Home NDC 83524-938 Dermoia Seborrheic Dermatitis Selenium Sulfide
Product NDC 83524-938
11-digit product format 835240938
Labeler code 83524
Product ID 83524-938_54e80d50-1487-eeec-e063-6294a90a6bf3
Type HUMAN OTC DRUG
Nonproprietary name SELENIUM SULFIDE
Dosage form SHAMPOO
Route TOPICAL
Labeler TREASUREWISE LLC
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-16
Substance SELENIUM SULFIDE
Active strength 10 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 Dermoia Seborrheic Dermatitis Selenium Sulfide
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SELENIUM SULFIDE 10 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination Z69D9E381Q Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 204642 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 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 83524-938-00 83524093800 355 mL in 1 BOTTLE (83524-938-00) 355 ml 2026-06-16 No No Current