Home NDC 83524-965 Dermoia Dandruff
Product NDC 83524-965
11-digit product format 835240965
Labeler code 83524
Product ID 83524-965_50095406-028b-71a7-e063-6294a90ae3c2
Type HUMAN OTC DRUG
Nonproprietary name PYRITHIONE ZINC
Dosage form SHAMPOO
Route TOPICAL
Labeler Treasurewise LLC
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-04-14
Substance PYRITHIONE ZINC
Active strength 15 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 Dandruff
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PYRITHIONE ZINC 15 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R953O2RHZ5 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 426904 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 83524-965-00 Dermoia Dandruff 355 mL in 1 BOTTLE SHAMPOO 355 1
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.
DailyMed RxNorm Mappings# Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 83524-965-00 83524096500 355 mL in 1 BOTTLE (83524-965-00) 355 ml 2026-04-14 No No Current