Home NDC 12022-034 Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil Serum
Product NDC 12022-034
11-digit product format 120220034
Labeler code 12022
Product ID 12022-034_0834f4b7-cae4-182f-e063-6294a90a7faa
Type HUMAN OTC DRUG
Nonproprietary name SULFUR
Dosage form SUSPENSION
Route TOPICAL
Labeler J. Strickland and Co.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance SULFUR
Active strength 25 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 Scalp Oil Serum
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SULFUR 25 mg/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 70FD1KFU70 Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 247683 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 12022-034-00 Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil Serum 81 mL in 1 BOTTLE SUSPENSION 81 3 12022-034-00 Sulfur 8 Scalp Therapy Medicated Dandruff Control Scalp Oil Serum 1 in 1 BOX SUSPENSION 1 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12022-034 SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL SCALP OIL SERUM (SULFUR) SUSPENSION [J. STRICKLAND AND CO.] 3 Current NDC, Legacy NDC, 2 package rows 20231021_96b249a2-3f50-1ab8-e053-2995a90a56ed.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 22 of 31 · 615 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Quality Choice Dandruff 2 in 1 PYRITHIONE ZINC CHAIN DRUG MARKETING ASSOCIATION, INC. 2c6289a3-2f09-c094-e063-6394a90a81f9 2025-01-23 Warnings Exact identifier application number: M032 Tuymec Anti-Fungal Shampoo. ANTI-FUNGAL SHAMPOO Guangzhou Zanming Trading Co., Ltd. 2c62d04e-dcb6-a33e-e063-6394a90a2e8e 2025-01-23 Warnings Exact identifier application number: M032 QC Anti Dandruff T Plus COAL TAR Chain Drug Marketing Association, Inc. 2bea5414-c7bc-d010-e063-6294a90aa138 2025-01-17 Warnings Exact identifier application number: M032 Meijer Medicated Selenium Sulfide Anti-Dandruff SELENIUM SULFIDE Meijer Distribution, Inc 41b563c6-5df6-4ead-bddf-a69a07970ea0 2025-01-14 Warnings Exact identifier application number: M032 D-COL Personal Hygiene Convenience kit PYRITHIONE ZINC AND CHLOROXYLENOL D-COL Inc 273fcc6f-9c54-42b0-aa0c-9051457b1341 2025-01-14 Warnings Exact identifier application number: M032 Equate Mens Ultra Sport 2 in 1 Dandruff SH and COND Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. f8767db7-e208-4ccc-85f7-789e281c7f26 2025-01-10 Warnings Exact identifier application number: M032 Equate Soft and Smooth 2 in 1 Dandruff SH and COND Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. c759b347-bdfb-4ff5-a464-b40fa2efb843 2025-01-10 Warnings Exact identifier application number: M032 Equate Mens Bold Scent 2 in 1 Dandruff SH and COND Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. d561e8d2-2761-422b-8f05-ac76d3a043eb 2025-01-10 Warnings Exact identifier application number: M032 Royal Oils by Head and Shoulders Sulfate Free Scalp Care PYRITHIONE ZINC The Procter & Gamble Manufacturing Company d73ab807-027f-7581-e053-2995a90ada83 2025-01-08 Warnings Exact identifier application number: M032 Head and Shoulders Supreme Color Protect Conditioner PYRITHIONE ZINC The Procter & Gamble Manufacturing Company 86ac3037-9ff2-25ea-e053-2a91aa0a43e3 2025-01-08 Warnings Exact identifier application number: M032 Oribe Serene Scalp Anti Dandruff ORIBE SERENE SCALP ANTI DANDRUFF Oribe Hair Care LLC e5702ac7-e680-ab4b-e053-2995a90ad442 2025-01-01 Warnings Exact identifier application number: M032 Oribe Serene Scalp Anti Dandruff ORIBE SERENE SCALP ANTI DANDRUFF Oribe Hair Care LLC abaf1c64-1c4d-481a-9872-b64fcf82cc63 2025-01-01 Warnings Exact identifier application number: M032 Dr. Groot Anti-dandruff Scalp Care SALICYLIC ACID TAI GUK PHARM. CO., LTD e8bdad4d-d499-70a9-e053-2a95a90a5cd9 2025-01-01 Warnings Exact identifier application number: M032 Dr. Groot Anti-dandruff Scalp Care 2 in 1 SALICYLIC ACID TAI GUK PHARM. CO., LTD e8bf3852-e963-7a48-e053-2995a90a5aa1 2025-01-01 Warnings Exact identifier application number: M032 American Crew PYRITHIONE ZINC Revlon Consumer Products Corp 9566b567-90be-4803-b940-e6a91750778f 2024-12-30 Warnings Exact identifier application number: M032 Kerastase Paris K Symbiose Serum Nuit Antipelliculaire Intensif Antidandruff Treatment SALICYLIC ACID L'Oreal USA Products Inc. d72688ed-d153-4eed-988f-5386eb68559d 2024-12-30 Warnings Exact identifier application number: M032 Dermaharmony Seborrheic Dermatitis PYRITHIONE ZINC D3 Development, Inc. 8d81521d-9e6f-1acf-e053-2995a90a9242 2024-12-20 Warnings Exact identifier application number: M032 Dermaharmony Sulfur and Salicylic Acid SALICYLIC ACID, SULFUR D3 Development, Inc. a1c61da2-7e7a-430a-e053-2995a90ad594 2024-12-20 Warnings Exact identifier application number: M032 Dermaharmony Bar Peppermint SALICYLIC ACID, SULFUR D3 Development, Inc. af7060a9-986c-500e-e053-2a95a90a6438 2024-12-20 Warnings Exact identifier application number: M032 Dermaharmony Bar Peppermint PYRITHIONE ZINC D3 Development, Inc. a19b74b0-88c6-6897-e053-2a95a90a7309 2024-12-20 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 12022-034-00 12022003400 1 BOTTLE in 1 BOX (12022-034-00) / 81 mL in 1 BOTTLE 1 bottle 2020-01-01 0000-00-00 No No Current