FDA.reportPublic FDA data

hair treatment

Manufacturer
LABORATORIO MK SRL | sonia organics
Effective date
2025-08-29
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:12:05

Label at a glance#

Producthair treatment
Active ingredientMINOXIDIL
Label structure8 sections

Label contents#

Full prescribing information#

INDICATIONS & USAGE SECTION

After washing the hair with EVOBEAUTY Minoxidil 1% Shampoo, apply evenly on wet hair, massage and leave on for 5 or 10 minutes. Rinse. directionsdirections

INACTIVE INGREDIENT SECTION

Water, Myristyl Alcohol, Hydroxycetyl Hydroxyethyl Dimonium Chloride, Isopropyl Myristate, Castor Oil, Cetrimonium Chloride, Behentrimonium Methosulfate (and) Cetearyl Alcohol, Cetyl Alcohol, Glycerin, Polyquaternium-7, Decyl Oleate, Ginger Root Extract, Peppermint Extract, Citric Acid, Benzyl Alcohol (and) Methylchloroisothiazolinone (and) Methylisothiazolinone ingredientsingredients

WARNINGS SECTION

Avoid eye contact, if occurs rinse eyes thoroughly with water. If develop any allergic reaction, discontinue its use. warningwarning

INFORMATION FOR OWNERS/CAREGIVERS SECTION

Customer Service USA (917)508-6002

Customer Service RD (809)379-0900

www.mkcosmeticos.com Customer Service USA (917)508-6002 Customer Service RD (809)379-0900 www.mkcosmeticos.comCustomer Service USA (917)508-6002 Customer Service RD (809)379-0900 www.mkcosmeticos.com

DOSAGE & ADMINISTRATION SECTION

After washing the hair with EVOBEAUTY Minoxidil 1% Shampoo, apply evenly on wet hair, massage and leave on for 5 or 10 minutes. Rinse. directionsdirections

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out reach of children. For external use only. warningwarning

OTC - PURPOSE SECTION

growth and help prevent hair and beard loss. Revitalizes hair follicles and stimulates growth.growth and help prevent hair and beard loss. Revitalizes hair follicles and stimulates growth.growth and help prevent hair and beard loss. Revitalizes hair follicles and stimulates growth.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

PRINCIPAL DISPLAY PANEL HAIR CREAMPRINCIPAL DISPLAY PANEL HAIR CREAMThis is the principal panel display side of the minoxidil hair cream 1%

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
MINOXIDIL Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
87022-009-25hair treatment473 mL in 1 JARCREAM4732

Products#

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

DailyMed product names page 1 of 1 · 19 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87022-00987022-009-25

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 18 matching rows.

Name, UNII, Kind table
NameUNIIKind
HYDROXYCETYL HYDROXYETHYL DIMONIUM CHLORIDE640X9A7H9NIACT
WATER059QF0KO0RIACT
CETEARYL ALCOHOL2DMT128M1SIACT
CETYL ALCOHOL936JST6JCNIACT
ISOPROPYL MYRISTATE0RE8K4LNJSIACT
BEHENTRIMONIUM METHOSULFATE5SHP745C61IACT
MINOXIDIL5965120SH1ACTIB
PEPPERMINTV95R5KMY2BIACT
.ALPHA.,.ALPHA.-DIMETHYLBENZYL ALCOHOLJE030BGE05IACT
CETRIMONIUM CHLORIDEUC9PE95IBPIACT
METHYLISOTHIAZOLINONE229D0E1QFAIACT
CASTOR OILD5340Y2I9GIACT
POLYQUATERNIUM-70L414VCS5YIACT
DECYL OLEATEZGR06DO97TIACT
CITRIC ACID2968PHW8QPIACT
GLYCERINPDC6A3C0OXIACT
GINGERC5529G5JPQIACT
METHYLCHLOROISOTHIAZOLINONEDEL7T5QRPNIACT

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
hair treatmentMINOXIDILLABORATORIO MK SRL3cf60fba-8c8d-d56f-e063-6294a90a344b2025-08-29WarningsExact identifier
ndc (package): 87022-009-25
ndc (product): 87022-009
ndc11 (package): 87022000925
spl id: 3d84eb2d-f0a8-a21c-e063-6294a90aeef5
spl set id: 3cf60fba-8c8d-d56f-e063-6294a90a344b

Reported adverse events (FAERS/openFDA)#

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