Home NDC 69423-349 Head and Shoulders Supreme Soothe and Strengthen Conditioner
Product NDC 69423-349
11-digit product format 694230349
Labeler code 69423
Product ID 69423-349_4640cbad-15b3-217c-e063-6394a90aeef0
Type HUMAN OTC DRUG
Nonproprietary name Pyrithione Zinc
Dosage form LOTION
Route TOPICAL
Labeler The Procter & Gamble Manufacturing Company
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2019-05-02
Substance PYRITHIONE ZINC
Active strength .5 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 Head and Shoulders Supreme Soothe and Strengthen Conditioner
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength PYRITHIONE ZINC .5 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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 1043014 Internal RxNorm lookup 1044465 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 69423-349-27 Head and Shoulders Supreme Soothe and Strengthen Conditioner 278 mL in 1 TUBE LOTION 278 7 69423-349-83 Head and Shoulders Supreme Soothe and Strengthen Conditioner 835 mL in 1 BOTTLE, PUMP LOTION 835 7
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-349 HEAD AND SHOULDERS SUPREME SOOTHE AND STRENGTHEN CONDITIONER (PYRITHIONE ZINC) LOTION [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 6 Current NDC, Legacy NDC, 2 package rows 20241129_86abfdc2-d55b-4adb-e053-2991aa0a54b1.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 69423-349-27 69423034927 278 mL in 1 TUBE (69423-349-27) 278 ml 2019-05-02 0000-00-00 No No Current 69423-349-83 69423034983 835 mL in 1 BOTTLE, PUMP (69423-349-83) 835 ml 2023-01-15 No No Current