FDA.reportPublic FDA data

SOLUCION CAPILAR CRECEPELO

Manufacturer
BOE Dominicana SRL
Effective date
2024-06-24
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 21:00:02

Label at a glance#

ProductSOLUCION CAPILAR CRECEPELO
Active ingredientMINOXIDIL
Label structure8 sections

Label contents#

Full prescribing information#

DOSAGE & ADMINISTRATION SECTION

DOSAGE AND ADMINISTRATION

take only as directed

WARNINGS SECTION

SKIN: Here are no known effects on contact with Skin, in case of irritation, rinse with water for a few minutes. Get medical attention if Irritation persists. INGESTION: Drink plenty of water and consult your doctor.

INACTIVE INGREDIENT SECTION

WATER PURIFIED S.C.P. ETHYIL ALCOHOL 30 PROPYLENGLYCOL 25 LACTIC ACID 1.0 TRITICUM VULGARE GLYCINE SOJA/EXCTRAT 0.5 FRAGRANCE 0.02 TETRASODIUM EDTA

INDICATIONS & USAGE SECTION

use as directed

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away. Quick medical attention is critical for adults as well as for children even if you do not notice any signs or symptoms

OTC - PURPOSE SECTION

Uses

HAIR REGROWTH TREATMENT

OTC - ACTIVE INGREDIENT SECTION

MINOXIDIL 5%

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

1122

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
78192-400SOLUCION CAPILAR CRECEPELO (MINOXIDIL) LIQUID [BOE DOMINICANA SRL]1Unmatched20240627_1ba6e2b6-14e2-0275-e063-6294a90a278d.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 9 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78192-40078192-400-01

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 8 matching rows.

Name, UNII, Kind table
NameUNIIKind
MINOXIDIL5965120SH1ACTIB
LACTIC ACID33X04XA5ATIACT
EDETATE SODIUMMP1J8420LUIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
WHEAT SPROUT3K32950CI0IACT
FRAGRANCE 135765EM498GW35IACT
ALCOHOL3K9958V90MIACT
WATER059QF0KO0RIACT

Source Document#

Source XML

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.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
3d748431-4419-7fed-e063-6394a90a65eb1ba6e2b6-14e2-0275-e063-6294a90a278d2025-08-28WarningsExact identifier
spl set id: 1ba6e2b6-14e2-0275-e063-6294a90a278d

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.