Home NDC 69423-526-40 Head and Shoulders Clinical Strength Dandruff Defense Intensive Itch Relief
Product NDC 69423-526
Requested package NDC 69423-526-40
11-digit product format 694230526
Labeler code 69423
Product ID 69423-526_47445198-5957-bfeb-e063-6394a90a9169
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 2020-11-17
Marketing end 2026-12-01
Substance SELENIUM SULFIDE
Active strength 1 g/100mL
NDC exclude flag No
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 · 3 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 2022-08-30 03:57 UTC · source 2022-08-29 excluded package package 69423-526 69423-526-40 I Inactivated by FDA excluded / ndc_excluded.zip fb8cb913e6d1…eb8c232b6be0…2022-04-09 23:13 UTC · source 2022-04-08 excluded package package 69423-526 69423-526-40 I Inactivated by FDA excluded / ndc_excluded.zip 86f5da6cb304…a595104c45d7…2022-04-04 05:40 UTC · source 2022-04-01 excluded package package 69423-526 69423-526-40 I Inactivated by FDA excluded / ndc_excluded.zip bd6a592717d7…303034d00443…
Additional Listing Data#
Finished product Yes
Brand name base Head and Shoulders Clinical Strength Dandruff Defense Intensive Itch Relief 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.
FDA-Initiated Inactive NDC Indexing# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 69423-526-01 Head and Shoulders Clinical Strength Dandruff Defense Intensive Itch Relief 2 in 1 CELLO PACK LOTION/SHAMPOO 2 5 69423-526-01 Head and Shoulders Clinical Strength Dandruff Defense Intensive Itch Relief 400 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 400 5 69423-526-40 Head and Shoulders Clinical Strength Dandruff Defense Intensive Itch Relief 400 mL in 1 BOTTLE, PLASTIC LOTION/SHAMPOO 400 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 69423-526 HEAD AND SHOULDERS CLINICAL STRENGTH DANDRUFF DEFENSE INTENSIVE ITCH RELIEF (SELENIUM SULFIDE) LOTION/SHAMPOO [THE PROCTER & GAMBLE MANUFACTURING COMPANY] 4 Current NDC, Legacy NDC, 3 package rows 20241027_b6ad7707-9d02-31a6-e053-2a95a90ae7ad.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 69423-526-40 69423052640 400 mL in 1 BOTTLE, PLASTIC (69423-526-40) 400 ml 2020-11-17 2026-12-01 No No Current