Home NDC 12022-033 Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment
Product NDC 12022-033
11-digit product format 120220033
Labeler code 12022
Product ID 12022-033_0834f4b7-cad7-182f-e063-6294a90a7faa
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form SOLUTION
Route TOPICAL
Labeler J. Strickland and Co.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance SALICYLIC ACID
Active strength 30 mg/mL
NDC exclude flag No
Listing certified through 2027-12-31
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 Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 30 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination O414PZ4LPZ Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 251294 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 12022-033-00 Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment 74 mL in 1 BOTTLE SOLUTION 74 3 12022-033-00 Sulfur 8 Scalp Therapy Medicated Dandruff Control Leave-In Soothing Treatment 1 in 1 BOX SOLUTION 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12022-033 SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL LEAVE-IN SOOTHING TREATMENT (SALICYLIC ACID) SOLUTION [J. STRICKLAND AND CO.] 3 Current NDC, Legacy NDC, 2 package rows 20231021_96b24a6f-3d6e-6d60-e053-2a95a90a8330.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 18 of 31 · 615 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Head and Shoulders Bare Minimal Ingredients Itchy Scalp Relief Serum PYRITHIONE ZINC The Procter & Gamble Manufacturing Company 402e2561-e309-46f2-e063-6394a90a4e58 2025-10-02 Warnings Exact identifier application number: M032 J1002902 Jason Dandruff Relief 2in1 Treatment PYRITHIONE ZINC The Hain Celestial Group Inc 8c631014-3832-78cb-e053-2995a90a8d22 2025-10-01 Warnings Exact identifier application number: M032 iBeaLee 5% Minoxidil Hair Regrowth Solution MINOXIDIL Shenzhen Earth Surface Trading Co., Ltd. 40001edd-d98c-4e2a-e063-6394a90a9911 2025-09-30 Warnings Exact identifier application number: M032 Head and Shoulders Dry Scalp Complete Hydration 2in1 PYRITHIONE ZINC The Procter & Gamble Manufacturing Company 3f66839a-0d8f-e476-e063-6294a90a547c 2025-09-22 Warnings Exact identifier application number: M032 5% MINOXIDIL HAIR REGROWTH SERUM With Biotin MINOXIDIL Shenzhen Ctrip Technology Co., Ltd. 1eae27bc-1b18-ae5d-e063-6394a90a4610 2025-09-12 Warnings Exact identifier application number: M032 Head and Shoulders Clinical Strength Dandruff Defense Advanced Oil Control SELENIUM SULFIDE The Procter & Gamble Manufacturing Company b6ad107b-024b-828f-e053-2995a90aae36 2025-09-04 Warnings Exact identifier application number: M032 Hermon Folliculitis Shampoo. SALICYLIC ACID 2% Beautivity LLC 3c5f7caa-a4af-2574-e063-6394a90a7507 2025-08-14 Warnings Exact identifier application number: M032 Pert 2 in 1 Advanced plus SALICYLIC ACID Sodalis USA, LLC 0eaed46c-ae6f-0d58-e063-6394a90ad2a3 2025-08-13 Warnings Exact identifier application number: M032 RoyceDerm Seborrheic Dermatitis and Dandruff Medicated Cleansing Bar PYRITHIONE ZINC 2% RoyceDerm LLC 3b98a83d-9c3b-9522-e063-6294a90a7033 2025-08-05 Warnings Exact identifier application number: M032 Earthmed FS Psoriasis relief SALICYLIC ACID Earthmed LLC 3ba584bc-f40a-ce0a-e063-6394a90aebf7 2025-08-05 Warnings Exact identifier application number: M032 Pert 2 in 1 Extra Strength SALICYLIC ACID Sodalis USA, LLC 25c8a46c-4400-709f-e063-6394a90a3f31 2025-07-30 Warnings Exact identifier application number: M032 anti-fungal ANTI-FUNGAL SHAMPOO GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd 3b102d15-f2ce-5727-e063-6294a90a23a9 2025-07-29 Warnings Exact identifier application number: M032 Earthmed Sport Anti itch and eczema relief SALICYLIC ACID Earthmed LLC 3b14913b-3aab-9dd0-e063-6394a90a3b7f 2025-07-29 Warnings Exact identifier application number: M032 Soothing psoriasis and eczema relief SALICYLIC ACID Carolina Cannabis Creations L.L.C 2bcad94d-1918-7f37-e063-6294a90a4744 2025-07-29 Warnings Exact identifier application number: M032 DANDRX ANTI-DANDRUFF ZINC PYRITHIONE dandRX LLC 399fb507-2263-962f-e063-6394a90ae9a8 2025-07-10 Warnings Exact identifier application number: M032 anti-dandruff ANTI-DANDRUFF SHAMPOO GUANGZHOU YUSONG FINE CHEMICLS Co., Ltd 3979fb80-8091-c79e-e063-6394a90ae618 2025-07-09 Warnings Exact identifier application number: M032 CeraVe 2 in 1 Anti-Dandruff Hydrating Conditioner PYRITHIONE ZINC LOreal USA Products Inc 7f5ff142-15cb-44be-aa0e-ccd06de23300 2025-07-08 Warnings Exact identifier application number: M032 5% Minoxidil and 5% Rosemary for Hair Care MINOXIDIL TIKNOW LLC 1bb386d2-70c6-c487-e063-6294a90a19da 2025-07-07 Warnings Exact identifier application number: M032 Red Scalpfixer Anti Dandruff PYRINTHIONE ZINC Orange Lab, Inc 386c83c3-8d23-b3b0-e063-6394a90a27ee 2025-07-01 Warnings Exact identifier application number: M032 Dermabon Multi Symptom Psoriasis Control COAL TAR Dermabon de Chihuahua, S.A. de C.V. d5b739ba-e332-41f6-9343-6ad5cc981344 2025-07-01 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 12022-033-00 12022003300 1 BOTTLE in 1 BOX (12022-033-00) / 74 mL in 1 BOTTLE 1 bottle 2020-01-01 0000-00-00 No No Current