Home NDC 12022-032 Sulfur 8 Scalp Therapy Medicated Dandruff Control
Product NDC 12022-032
11-digit product format 120220032
Labeler code 12022
Product ID 12022-032_0834eb14-2e95-ef47-e063-6294a90ad922
Type HUMAN OTC DRUG
Nonproprietary name SALICYLIC ACID
Dosage form SPRAY
Route TOPICAL
Labeler J. Strickland and Co.
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2020-01-01
Substance SALICYLIC ACID
Active strength 20 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
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength SALICYLIC ACID 20 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 1048903 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 12022-032-00 Sulfur 8 Scalp Therapy Medicated Dandruff Control 355 mL in 1 BOTTLE SPRAY 355 3
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 12022-032 SULFUR 8 SCALP THERAPY MEDICATED DANDRUFF CONTROL (SALICYLIC ACID) SPRAY [J. STRICKLAND AND CO.] 3 Current NDC, Legacy NDC, 1 package rows 20231021_961ffab9-4e1b-83f3-e053-2a95a90af5fe.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 25 of 31 · 615 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join Meijer T Plus Gel Coal Tar Anti-Dandruff COAL TAR Meijer Distribution, Inc c4b0d6e5-0756-45e8-bdfc-a8ba728b246b 2024-11-05 Warnings Exact identifier application number: M032 Walgreens Dandruff Conditioner 2 in 1 Itchy Scalp Anti-dandruff PYRITHIONE ZINC Walgreen Company 52594e2b-dd1b-4618-b1ab-9f65ae26a358 2024-11-04 Warnings Exact identifier application number: M032 Walgreens Dandruff Plus Conditioner 2 in 1 Anti-dandruff PYRITHIONE ZINC Walgreen Company 12ccb5aa-4e0d-467b-a03c-dddd6da0a9c9 2024-11-04 Warnings Exact identifier application number: M032 Walgreens Dandruff Plus Conditioner 2 in 1 Dry Scalp Anti-dandruff PYRITHIONE ZINC Walgreen Company 0fed00b3-cac6-4add-b979-a3fe112bcff3 2024-11-04 Warnings Exact identifier application number: M032 Walgreens Dandruff Itchy Dry Scalp Defense Anti-dandruff PYRITHIONE ZINC Walgreen Company 06b37d44-9ebf-44ed-8e8b-492905d85bdc 2024-11-01 Warnings Exact identifier application number: M032 Walgreens Dandruff Conditioner 2 in 1 Itchy Scalp Anti-dandruff PYRITHIONE ZINC Walgreen Company 5b679112-8790-416f-9bb4-8e64d3e279bc 2024-11-01 Warnings Exact identifier application number: M032 Walgreens Dandruff Itchy Dry Scalp Defense Plus Vitamins and Botanicals Anti-dandruff SALICYLIC ACID Walgreen Company 2776d45c-6597-4c13-81e6-29d9248e9e56 2024-11-01 Warnings Exact identifier application number: M032 Walgreens Dandruff and Conditioner Cleansing and Conditioning Anti-dandruff SELENIUM SULFIDE Walgreen Company dbcaeae8-4680-41d8-84e2-896183d2121d 2024-11-01 Warnings Exact identifier application number: M032 Walgreens Dandruff Maximum Strength Anti-dandruff SELENIUM SULFIDE Walgreen Company 0187b034-44d7-4b84-af04-d018bc9750f3 2024-11-01 Warnings Exact identifier application number: M032 Dermarest Psoriasis Medicated SALICYLIC ACID Insight Pharmaceuticals LLC c6a64946-bafd-449f-90cc-e2f6201285f3 2024-10-25 Warnings Exact identifier application number: M032 DermaSolve Medicated SALICYLIC ACID Fortitude Health, LLC 253e2687-6e8b-48ec-e063-6394a90aa20b 2024-10-24 Warnings Exact identifier application number: M032 FAMILY Wellness FRESH and CLEAN DANDRUFF PLUS CONDITIONER 2 IN 1 Anti-Dandruff PYRITHIONE ZINC FAMILY DOLLAR SERVICES INC 4a9a803a-44ac-4e29-9c47-0073b728ff19 2024-10-22 Warnings Exact identifier application number: M032 DermaSolve Medicated SALICYLIC ACID Fortitude Health, LLC 24fea3b2-1f0a-e289-e063-6394a90a5641 2024-10-21 Warnings Exact identifier application number: M032 FAMILY Wellness EVERYDAY CLEAN 2 IN 1 DANDRUFF PLUS CONDITIONER Anti-Dandruff PYRITHIONE ZINC FAMILY DOLLAR SERVICES INC 220955ec-592c-421f-9f4e-545ff3843ee0 2024-10-21 Warnings Exact identifier application number: M032 FAMILY Wellness MAXIMUM STRENGTH DANDRUFF Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis SELENIUM SULFIDE FAMILY DOLLAR SERVICES INC 41a808e1-67a7-4b29-8ec4-d6c13cf62243 2024-10-21 Warnings Exact identifier application number: M032 Family Wellness Therapeutic Tplus PLUS Dandruff Anti-dandruff, anti-seborrheic dermatitis, anti-psoriasis COAL TAR FAMILY DOLLAR SERVICES INC 46471dfa-2322-464f-8d00-bf49d8eb4e18 2024-10-21 Warnings Exact identifier application number: M032 As I Am Dry and Itchy Scalp Care Conditioner PYRITHIONE ZINC Salon Commodities, Inc. 71eb9451-df12-66e8-e053-2a95a90a2f69 2024-10-09 Warnings Exact identifier application number: M032 As I Am Dry and Itchy Scalp Care Treatment SALICYLIC ACID Salon Commodities, Inc. 71ec25c5-6da5-670a-e053-2a95a90a1b8c 2024-10-09 Warnings Exact identifier application number: M032 KeraCare Dry and Itchy Scalp Anti-Dandruff PYRITHIONE ZINC Avlon Industries, Inc. 6e7524d7-b280-485a-815e-8af078e8acda 2024-10-09 Warnings Exact identifier application number: M032 KeraCare Dry and Itchy Scalp Anti-Dandruff PYRITHIONE ZINC Avlon Industries, Inc. 5d501ba0-a6f9-4f0d-86d5-0e8d9302737f 2024-10-09 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 12022-032-00 12022003200 355 mL in 1 BOTTLE (12022-032-00) 355 ml 2020-01-01 0000-00-00 No No Current