Home NDC 87813-001 Minoxidil Hair Regrowth Kit
Product NDC 87813-001
11-digit product format 878130001
Labeler code 87813
Product ID 87813-001_550bce76-4c79-80f0-e063-6394a90ad58f
Type HUMAN OTC DRUG
Nonproprietary name Minoxidil
Dosage form LIQUID
Route TOPICAL
Labeler Guangzhou Zeus E-commerce Co., Ltd
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-06-25
Substance MINOXIDIL
Active strength .05 g/mL
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 Minoxidil Hair Regrowth Kit
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL .05 g/mL
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 RxCUI identifiers# RxCUI identifiers page 1 of 1 · 1 matching rows.
Identifier, FDA.report destination table Identifier FDA.report destination 311724 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 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 87813-001-01 87813000101 4 BOTTLE in 1 BOX (87813-001-01) / 30 mL in 1 BOTTLE 4 bottle 2026-06-25 No No Current