Home NDC 12022-007 Glovers Dandruff Control Medicine, Regular
Product NDC 12022-007
11-digit product format 120220007
Labeler code 12022
Product ID 12022-007_08340897-23b3-f23b-e063-6294a90a4eb9
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 2001-09-24
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 Medicine, Regular
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 Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 12022-007-00 Glovers Dandruff Control Medicine, Regular 81 mL in 1 BOTTLE SUSPENSION 81 5 12022-007-00 Glovers Dandruff Control Medicine, Regular 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 12022-007 GLOVERS DANDRUFF CONTROL MEDICINE, REGULAR (SULFUR) SUSPENSION [J. STRICKLAND & CO.] 5 Current NDC, Legacy NDC, 2 package rows 20231021_18700036-11ec-4370-bcc6-b9e2c732e7d9.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 12022-007-00 12022000700 1 BOTTLE in 1 CARTON (12022-007-00) / 81 mL in 1 BOTTLE 1 bottle 2001-09-24 0000-00-00 No No Current