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 32 · 630 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join SMOOTH AND SOFT DANDRUFF PYRITHIONE ZINC Universal Distribution Center LLC 9e235139-07a2-469a-8601-db69379ce347 2026-08-24 Warnings Exact identifier application number: M032 ITCHY SCALP RELIEF DANDRUFF PYRITHIONE ZINC Universal Distribution Center LLC 634019c2-03a3-4fed-939e-6f9a50ddea7b 2026-08-24 Warnings Exact identifier application number: M032 Minoxidil Hair Regrowth Treatment MINOXIDIL Shenzhen Earth Surface Trading Co., Ltd. 59b4f9e3-c241-6a70-e063-6294a90a364f 2026-08-23 Warnings Exact identifier application number: M032 Minoxidil Hair Regrowth Treatment MINOXIDIL Shenzhen Earth Surface Trading Co., Ltd. 59b52a52-dab0-87b5-e063-6294a90a0596 2026-08-23 Warnings Exact identifier application number: M032 Minoxidil Hair Regrowth Treatment MINOXIDIL Shenzhen Earth Surface Trading Co., Ltd. 59b67ce0-3546-c18a-e063-6394a90ae50a 2026-08-23 Warnings Exact identifier application number: M032 Anti Dandruff KETOCONAZOLE Guangzhou ChuanMa International Trading Co.,Ltd. 599f2cce-0c27-d425-e063-6394a90a1565 2026-08-22 Warnings Exact identifier application number: M032 Anti Dandruff KETOCONAZOLE Guangzhou ChuanMa International Trading Co.,Ltd. 59a0a062-92d1-210a-e063-6394a90a9bf9 2026-08-22 Warnings Exact identifier application number: M032 Ouai Anti-Dandruff SALICYLIC ACID The Procter & Gamble Manufacturing Company 5990c45f-f653-b403-e063-6394a90a329d 2026-08-21 Warnings Exact identifier application number: M032 Dermatology Psoriasis Cream COAL TAR G.M.J Natural Products, Inc. 96cc5455-f3b8-4ded-a158-5de209d7bf0d 2026-08-21 Warnings Exact identifier application number: M032 apgwgzminoxidil5% MINOXIDIL Guangdong Jiaoyu Biotechnology Co., Ltd 596d0b43-5cb1-be25-e063-6394a90abbed 2026-08-19 Warnings Exact identifier application number: M032 TEA TREE Oil DANDRUFF PYRITHIONE ZINC Universal Distribution Center LLC 280391ce-ccd9-4b39-95a2-93e7fca84ccc 2026-08-18 Warnings Exact identifier application number: M032 apgwgzminoxidil2% MINOXIDIL Guangdong Jiaoyu Biotechnology Co., Ltd 5957c990-e274-6278-e063-6394a90af2b7 2026-08-18 Warnings Exact identifier application number: M032 EVERYDAY CLEAN DANDRUFF PYRITHIONE ZINC Universal Distribution Center LLC 3983b688-28ae-462e-8686-6cf2f2c1cca4 2026-08-18 Warnings Exact identifier application number: M032 Prosoria Psoriasis Treatment SALICYLIC ACID Nuvothera, Inc. 378311aa-95f7-4c69-bc00-e688468262bd 2026-08-18 Warnings Exact identifier application number: M032 RoyceDerm Seborrheic Dermatitis and Psoriasis Treatment cream SALICYLIC ACID 3% RoyceDerm LLC 496e178b-e29b-071e-e063-6394a90aa018 2026-08-13 Warnings Exact identifier application number: M032 RoyceDerm Seborrheic Dermatitis and Psoriasis shampoo. SALICYLIC ACID 3% RoyceDerm LLC 4995ce33-e231-8f86-e063-6394a90af486 2026-08-13 Warnings Exact identifier application number: M032 Rida Hair Research Institute RHRI Neoketramin Antifungal Yeast Relief PYRITHIONE ZINC Rida LLC d1e4dee7-5962-4ec1-ab99-9d547077b2f2 2026-08-05 Warnings Exact identifier application number: M032 Rida Hair Research Institute RHRI Neoketramin Antifungal Yeast Relief Treatment SALICYLIC ACID Rida LLC 6226ce12-432f-402e-bda7-a5ca96f0b838 2026-08-05 Warnings Exact identifier application number: M032 JOHNSON FOAM MINOXIDIL JOHNSON BIOPHARMACEUTICAL INC. 1d44a75c-c940-680c-e063-6394a90a5839 2026-08-02 Warnings Exact identifier application number: M032 FOLKI COSMETIC Psoriasis Cream SALICYLIC ACID 3% PSORIASIS CREAM Wenzhou Yuyuan Pharmaceutical Co., Ltd. 575786e0-21b8-ad9d-e063-6394a90ad0d4 2026-07-24 Warnings Exact identifier application number: M032
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