FDA.reportPublic FDA data

marry skin Be Hairful

Manufacturer
YEGREENA CO., LTD.
Effective date
2020-09-16
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:13

Label at a glance#

Productmarry skin Be Hairful
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.1%

OTC - PURPOSE SECTION

Anti-dandruff

INDICATIONS & USAGE SECTION

Helps prevent recurrence of flaking and itching associated with dandruff

DOSAGE & ADMINISTRATION SECTION

- Thoroughly wet hair from roots to ends lukewarm water.  Lather moderate amounts of shampoo and massage scalp and hair using fingers or application.
- Rinse with water to clean hair.

WARNINGS SECTION

For external use only.
When using this product, do not get into eyes. If contact occurs, rinse eyes thoroughly with water.

Stop use and ask a doctor if condition worsens or does not improve after regular use as directed.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of the children. If product is swallowed, get medical help or contact a poison control center right away.

INACTIVE INGREDIENT SECTION

Water, Sodium C14-16 Olefin Sulfonate, Cocamidopropyl Hydroxysultaine, Lauryl Glucoside, Decyl Glucoside, Guar Hydroxypropyltrimonium Chloride, Coco-glucoside, Fragrance , Sodium chloride, Methylpropanediol, Citric Acid, Butylene Glycol, Panthenol, Niacinamide, Glyceryl Caprylate, Climbazole, Ethylhexylglycerin, Saccharomyces Cerevisiae Extract , Monarda Didyma Leaf Extract, Mentha Piperita (Peppermint) Leaf Extract, Freesia Refracta Extract, Chamomilla recutita (Matricaria) flower Extract, Rosmarinus Officinalis (Rosemary) Leaf Extract, Lavandula Angustifolia (Lavender) Flower Extract, 1,2-Hexanediol, Disodium EDTA

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage description

Products#

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

DailyMed product names page 1 of 1 · 27 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78417-00378417-003-01, 78417-003-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 25 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
SODIUM C14-16 OLEFIN SULFONATEO9W3D3YF5UIACT
COCAMIDOPROPYL HYDROXYSULTAINE62V75NI93WIACT
LAURYL GLUCOSIDE76LN7P7UCUIACT
DECYL GLUCOSIDEZ17H97EA6YIACT
GUAR HYDROXYPROPYLTRIMONIUM CHLORIDE (1.7 SUBSTITUENTS PER SACCHARIDE)B16G315W7AIACT
COCO GLUCOSIDEICS790225BIACT
SODIUM CHLORIDE451W47IQ8XIACT
METHYLPROPANEDIOLN8F53B3R4RIACT
CITRIC ACID MONOHYDRATE2968PHW8QPIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
PANTHENOLWV9CM0O67ZIACT
NIACINAMIDE25X51I8RD4IACT
GLYCERYL MONOCAPRYLATETM2TZD4G4AIACT
CLIMBAZOLE9N42CW7I54IACT
ETHYLHEXYLGLYCERIN147D247K3PIACT
SACCHAROMYCES CEREVISIAE978D8U419HIACT
MONARDA DIDYMA LEAFJY15982UBBIACT
MENTHA PIPERITA LEAFA389O33LX6IACT
CHAMOMILEFGL3685T2XIACT
ROSEMARYIJ67X351P9IACT
LAVANDULA ANGUSTIFOLIA SUBSP. ANGUSTIFOLIA FLOWER19AH1RAF4MIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
SALICYLIC ACIDO414PZ4LPZACTIB

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
af8c0133-75b7-b1b0-e053-2a95a90adfb72917e30f-a399-49ea-b7ff-1165e034c8542020-09-17WarningsExact identifier
spl set id: 2917e30f-a399-49ea-b7ff-1165e034c854

Reported adverse events (FAERS/openFDA)#

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