Home NDC 69423-642 Head and Shoulders Clinical Strength Dandruff Defense Sensitive Scalp
Product NDC 69423-642
11-digit product format 694230642
Labeler code 69423
Product ID 69423-642_47454f58-395b-cc93-e063-6294a90a0640
Type HUMAN OTC DRUG
Nonproprietary name Selenium Sulfide
Dosage form LOTION/SHAMPOO
Route TOPICAL
Labeler The Procter & Gamble Manufacturing Company
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2022-04-22
Marketing end 2026-09-01
Substance SELENIUM SULFIDE
Active strength 1 g/100mL
NDC exclude flag No
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Head and Shoulders Clinical Strength Dandruff Defense Sensitive Scalp Active Ingredients# Ingredient, Strength table Ingredient Strength SELENIUM SULFIDE 1 g/100mL
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 · 2 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 204642 Internal RxNorm lookup 1549328 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 69423-642-40 Head and Shoulders Clinical Strength Dandruff Defense Sensitive Scalp 400 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 400 4
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-642 HEAD AND SHOULDERS CLINICAL STRENGTH DANDRUFF DEFENSE SENSITIVE SCALP (SELENIUM SULFIDE) LOTION/SHAMPOO [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 3 Current NDC, Legacy NDC, 1 package rows 20241030_eedc5e57-8047-eab7-e053-2a95a90a2e2a.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 1 of 31 · 617 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 69423-642-40 69423064240 400 mL in 1 BOTTLE, PLASTIC (69423-642-40) 400 ml 2022-04-22 2026-09-01 No No Current