Home NDC 41163-024-40 Dandruff
Product NDC 41163-024
Requested package NDC 41163-024-40
11-digit product format 411630024
Labeler code 41163
Product ID 41163-024_4b06c184-4d5b-4838-e063-6294a90a8176
Type HUMAN OTC DRUG
Nonproprietary name PYRITHIONE ZINC
Dosage form LOTION/SHAMPOO
Route TOPICAL
Labeler United Natural Foods, Inc. dba UNFI
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2006-10-26
Substance PYRITHIONE ZINC
Active strength 10 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
Current FDA listing Yes Observed NDC auxiliary status history# This history shows the information present in each captured FDA auxiliary file. It is not a continuous regulatory timeline, and a missing record does not establish a status.
Historic NDC status page 1 of 1 · 1 matching rows.
View current auxiliary records. · View the auxiliary file history.
Captured / source date, Dataset, Scope table Captured / source date Dataset Scope Product NDC Package NDC Code Status Reporting period Archive Snapshot Source SHA-256 2024-07-10 04:00 UTC · source 2024-07-09 excluded package package 41163-024 41163-024-40 D Discontinued by firm excluded / ndc_excluded.zip 557ba5c1ecfa…9c80585c8c6e…
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 Dandruff
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PYRITHIONE ZINC 10 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 209884 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 41163-024-15 Dandruff 420 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 420 16 41163-024-32 Dandruff 370 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 370 16 41163-024-35 Dandruff 700 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 700 16 41163-024-40 Dandruff 612 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 612 16
DailyMed Socrata Ingredients# DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 41163-024 DANDRUFF (PYRITHIONE ZINC) LOTION/SHAMPOO [UNITED NATURAL FOODS, INC. DBA UNFI] 14 Current NDC, Legacy NDC, 4 package rows 20250429_d7c4507e-7f74-4bcd-9b0e-0b097193a1a8.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 Sample Exclude flag Status 41163-024-40 41163002440 612 mL in 1 BOTTLE, PLASTIC (41163-024-40) 612 ml 2023-11-02 No No Current