Home NDC 87022-010 hair leave in
Product NDC 87022-010
11-digit product format 870220010
Labeler code 87022
Product ID 87022-010_3d84d7f8-a36c-bb37-e063-6394a90af897
Type HUMAN OTC DRUG
Nonproprietary name minoxidil
Dosage form CREAM
Route TOPICAL
Labeler LABORATORIO MK SRL
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2025-08-22
Marketing end 2027-08-20
Substance MINOXIDIL
Active strength 1 mg/234mL
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag No
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 hair leave in Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 1 mg/234mL
Harmonized UNII identifiers# UNII identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 5965120SH1 Internal UNII 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 87022-010-26 hair leave in 234 mL in 1 BOTTLE, PLASTIC CREAM 234 2
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 1 of 1 · 1 matching rows.
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 87022-010-26 87022001026 234 mL in 1 BOTTLE, PLASTIC (87022-010-26) 234 ml 2025-08-22 2027-08-20 Yes No Historical