Home NDC 78192-401 SOLUCION CAPILAR CRECEPELO
Product NDC 78192-401
11-digit product format 781920401
Labeler code 78192
Product ID 78192-401_3d490b9b-1c92-1b07-e063-6294a90a5355
Type HUMAN OTC DRUG
Nonproprietary name MINOXIDIL
Dosage form LIQUID
Route TOPICAL
Labeler BOE Dominicana SRL
Application 505G(a)(3)
Marketing category OTC MONOGRAPH DRUG
Marketing start 2024-06-25
Substance MINOXIDIL
Active strength 5 mg/30mL
Pharmacologic classes Arteriolar Vasodilation [PE], Arteriolar Vasodilator [EPC]
NDC exclude flag No
Listing certified through 2026-12-31
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 SOLUCION CAPILAR CRECEPELO
Listing expiration 2026-12-31 Active Ingredients# Ingredient, Strength table Ingredient Strength MINOXIDIL 5 mg/30mL
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 78192-401-01 SOLUCION CAPILAR CRECEPELO 23 mL in 1 BOTTLE, DROPPER LIQUID 23 2 78192-401-01 SOLUCION CAPILAR CRECEPELO 4 in 1 CARTON LIQUID 4 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 Marketing start Sample Exclude flag Status 78192-401-01 78192040101 4 BOTTLE, DROPPER in 1 CARTON (78192-401-01) / 23 mL in 1 BOTTLE, DROPPER 2024-06-25 No No Current