Home NDC 12022-008 Glovers Dandruff Control Med., Floral
Product NDC 12022-008
11-digit product format 120220008
Labeler code 12022
Product ID 12022-008_0833dce8-d162-c283-e063-6294a90a984a
Type HUMAN OTC DRUG
Nonproprietary name Sulfur
Dosage form SUSPENSION
Route TOPICAL
Labeler J. Strickland & Co.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2001-11-05
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 Glovers Dandruff Control Med., Floral
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 12022-008-00 Glovers Dandruff Control Med., Floral 81 mL in 1 BOTTLE SUSPENSION 81 5 12022-008-00 Glovers Dandruff Control Med., Floral 1 in 1 CARTON SUSPENSION 1 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12022-008 GLOVERS DANDRUFF CONTROL MED., FLORAL (SULFUR) SUSPENSION [J. STRICKLAND & CO.] 5 Current NDC, Legacy NDC, 2 package rows 20231021_a1224e4a-e811-4415-a038-3933da43d819.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 28 of 31 · 613 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join XtraCare Anti-Dandruff Hair Cleanse Coconut and Shea Butter PYRITHIONE ZINC Rejoice International Inc. 7d9bf611-db24-4915-9b13-b7b36f47711f 2024-02-28 Warnings Exact identifier application number: M032 XtraCare Anti-Dandruff Hair Cleanse mint and eucalyptus PYRITHIONE ZINC Rejoice International Inc. b05742fe-692f-45a3-9de0-5f3f08642d78 2024-02-28 Warnings Exact identifier application number: M032 XtraCare Dandruff Hair Wash SALICYLIC ACID Rejoice International 1902e6bb-e829-4b1a-b85a-1394913c77ca 2024-02-28 Warnings Exact identifier application number: M032 amazon basics maximum strength dandruff Anti-dandruff SELENIUM SULFIDE AMAZON.COM SERVICES LLC 194e4c51-ff7b-4def-a71d-efa5dfca3efd 2024-02-26 Warnings Exact identifier application number: M032 Doo Gro Braids Twists Locs Dandruff Control Moisturizing SALICYLIC ACID J. Strickland and Co. 116f4f0d-66c7-49dd-e063-6394a90ab2b5 2024-02-15 Warnings Exact identifier application number: M032 amazon basics therapeutic tar anti-dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR AMAZON.COM SERVICES LLC ada1be0c-53a7-443c-bc3c-f7a26b5f96a9 2024-02-05 Warnings Exact identifier application number: M032 Equate Dry Scalp 2 in 1 Dandruff Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. 6440fdd9-daa8-4f15-bdee-33724993bd7b 2024-02-01 Warnings Exact identifier application number: M032 Equate Everyday Clean Dandruff Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. 4c84a67a-1f43-4f40-a172-271de7e76785 2024-01-29 Warnings Exact identifier application number: M032 Equate Everyday Clean 2 in 1 Dandruff Anti-Dandruff PYRITHIONE ZINC Wal-Mart Stores, Inc. c85095f2-5dbd-4822-a83a-dc3641c4a330 2024-01-29 Warnings Exact identifier application number: M032 Hydrocortisone ANTIPRURITIC (ANTI-ITCH) Dynarex Corporation 81dff9df-6f7e-49f0-e053-2a91aa0af7e7 2024-01-23 Warnings Exact identifier application number: M032 Walgreens Original T-Gel Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Walgreen Company 42cc63ab-6f79-4544-8529-7b8c36021b18 2024-01-22 Warnings Exact identifier application number: M032 True plus Real Therapeutic T plus Plus Original Strength Tar Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Garcoa, Inc. 1f4c23d5-ca00-4387-abc7-59d9ef471977 2024-01-22 Warnings Exact identifier application number: M032 Walgreens Extra Strength T-Gel Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Walgreen Company 7f681386-976c-40f4-8b18-97413989ab78 2024-01-22 Warnings Exact identifier application number: M032 Prosoria Medicated SELENIUM SULFIDE Nuvothera, Inc. 44eaaeb0-1400-4697-85d0-e8c2282c1cba 2024-01-11 Warnings Exact identifier application number: M032 Prosoria Scalp SALICYLIC ACID Nuvothera, Inc. 52a98715-3e57-4b86-b91e-0ce433dc22bd 2024-01-10 Warnings Exact identifier application number: M032 Prosoria Psoriasis Treatment SALICYLIC ACID Nuvothera, Inc. f94f4481-c58e-4555-9863-cbaa2c4cdd07 2024-01-10 Warnings Exact identifier application number: M032 Equate Therapeutic Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Wal-Mart Stores, Inc. 408d57e4-a707-4826-a04c-99517dc9b5af 2024-01-04 Warnings Exact identifier application number: M032 Equate Extra Strength Therapeutic Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR Wal-Mart Stores, Inc. 986ac1ab-c7c3-40df-b41b-6f26cce22a43 2024-01-04 Warnings Exact identifier application number: M032 Pert Plus 2 in 1 Anti-Dandruff PYRITHIONE ZINC TCP HRB Holdings ecfa3d29-b54c-265c-e053-2995a90a8020 2024-01-01 Warnings Exact identifier application number: M032 CeraVe Developed with Dermatologists Psoriasis Moisturizing SALICYLIC ACID L'Oreal USA Products Inc 51f27970-92d3-44ae-b2b1-d820719680fe 2023-12-28 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 12022-008-00 12022000800 1 BOTTLE in 1 CARTON (12022-008-00) / 81 mL in 1 BOTTLE 1 bottle 2001-11-05 0000-00-00 No No Current