Home NDC 87408-033-01 FIGTORUS Minoxidil Hair Growth Treatment
Product NDC 87408-033
Requested package NDC 87408-033-01
11-digit product format 874080033
Labeler code 87408
Product ID 87408-033_5aa2db1d-dda9-b0d7-e063-6294a90a67a5
Type HUMAN OTC DRUG
Nonproprietary name Minoxidil Hair Growth Treatment
Dosage form AEROSOL, FOAM
Route TOPICAL
Labeler Guangzhou Jingliang Cosmetics Co., Ltd.
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2026-09-03
Substance MINOXIDIL
Active strength 5 g/100mL
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 FIGTORUS Minoxidil Hair Growth Treatment
Listing expiration 2027-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 g/100mL
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 645146 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 87408-033-01 87408003301 3 BOTTLE in 1 CARTON (87408-033-01) / 60 mL in 1 BOTTLE 3 bottle 2026-09-03 No No Current