Home NDC 87863-021 5% Minoxidil Topical Solution
Product NDC 87863-021
11-digit product format 878630021
Labeler code 87863
Product ID 87863-021_58e8f7a9-54a2-3db5-e063-6294a90a22e8
Type HUMAN OTC DRUG
Nonproprietary name 5% Minoxidil Topical Solution
Dosage form LOTION/SHAMPOO
Route CUTANEOUS
Labeler Shenzhen Jinyang E-commerce Business Department (A Sole Proprietorship)
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2026-08-01
Substance MINOXIDIL
Active strength 5 mg/100mg
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
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 5% Minoxidil Topical Solution
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 mg/100mg
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.
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 Sample Exclude flag Status 87863-021-01 87863002101 100 mg in 1 BOTTLE (87863-021-01) 100 mg 2026-08-01 No No Current