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 16 of 31 · 615 matching rows.
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