Home NDC 64724-1017 NATURALTECH PURIFYING ANTI-DANDRUFF
Product NDC 64724-1017
11-digit product format 647241017
Labeler code 64724
Product ID 64724-1017_28ff9fbd-1d80-1984-e063-6294a90abb69
Type HUMAN OTC DRUG
Nonproprietary name PYRITHIONE ZINC
Dosage form GEL
Route TOPICAL
Labeler Davines S.p.A.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2012-02-29
Substance PYRITHIONE ZINC
Active strength .48 g/100mL
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 NATURALTECH PURIFYING ANTI-DANDRUFF
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PYRITHIONE ZINC .48 g/100mL
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 1245937 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 64724-1017-1 NATURALTECH PURIFYING ANTI-DANDRUFF 1 in 1 CARTON GEL 1 5 64724-1017-1 NATURALTECH PURIFYING ANTI-DANDRUFF 150 mL in 1 BOTTLE GEL 150 5
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 64724-1017 NATURALTECH PURIFYING ANTI-DANDRUFF (PYRITHIONE ZINC) GEL [DAVINES S.P.A.] 5 Current NDC, Legacy NDC, 2 package rows 20241213_1f7e0265-0543-4ef9-addf-4d514d0eedfe.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 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 Marketing end Sample Exclude flag Status 64724-1017-1 64724101701 1 BOTTLE in 1 CARTON (64724-1017-1) / 150 mL in 1 BOTTLE 1 bottle 2012-02-29 0000-00-00 No No Current