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 31 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 12022-033-00 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