Home NDC 87880-001 5% Minoxidil Sprays HAIR EGROWTH TREATMENT
Product NDC 87880-001
11-digit product format 878800001
Labeler code 87880
Product ID 87880-001_57a3794d-b4a2-8ee8-e063-6294a90acb8a
Type HUMAN OTC DRUG
Nonproprietary name Minoxidil 5%
Dosage form LIQUID
Route TOPICAL
Labeler Tuosen Hong Kong Import Export Trading Co., Limited
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-07-23
Substance MINOXIDIL
Active strength .05 g/mL
Pharmacologic classes Arteriolar Vasodilation [PE]; Arteriolar Vasodilator [EPC]
Listing certified through 2027-12-31
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base 5% Minoxidil Sprays HAIR EGROWTH TREATMENT
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 1537948 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 Status 87880-001-01 87880000101 1 BOTTLE in 1 BOX (87880-001-01) / 60 mL in 1 BOTTLE 1 bottle 2026-07-23 0 Current