Home NDC 87722-069 ANTI DANDRUFF
Product NDC 87722-069
11-digit product format 877220069
Labeler code 87722
Product ID 87722-069_5ce89c87-d4ec-2d20-e063-6394a90aa971
Type HUMAN OTC DRUG
Nonproprietary name KETOCONAZOLE
Dosage form LIQUID
Route TOPICAL
Labeler Guangdong Jiaoyu Biotechnology Co., Ltd
Application M032
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-10-03
Substance KETOCONAZOLE
Active strength 1 mg/100mg
Pharmacologic classes Azole Antifungal [EPC], Azoles [CS], Cytochrome P450 3A4 Inhibitors [MoA], Cytochrome P450 3A5 Inhibitors [MoA], P-Glycoprotein Inhibitors [MoA]
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 ANTI DANDRUFF
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength KETOCONAZOLE 1 mg/100mg
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination R9400W927I Internal UNII lookup
Harmonized RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 240812 Internal RxNorm lookup
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
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 · 602 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Sample Exclude flag Status 87722-069-01 87722006901 200 mg in 1 BOTTLE (87722-069-01) 200 mg 2026-10-03 No No Current