FDA.reportPublic FDA data

marry skin Be Hairful Tonic

Manufacturer
YEGREENA CO., LTD.
Effective date
2020-09-17
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-01 23:15:10

Label at a glance#

Productmarry skin Be Hairful Tonic
Active ingredientSALICYLIC ACID
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Salicylic Acid 0.25%

OTC - PURPOSE SECTION

Anti-dandruff

INDICATIONS & USAGE SECTION

Helps prevent recurrence of flaking and itching associated with dandruff

DOSAGE & ADMINISTRATION SECTION

 Twice a day. Thoroughly shake hair tonic before use. Spray moderate amount of hair tonic and massage scalp using fingers absorbs well.

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, Butylene Glycol, Alcohol Denat., C12-14 Pareth-12, Menthol, Allantoin, Trehalose, Panthenol, Arginine, Melia Azadirachta Leaf Extract, Melia Azadirachta Flower Extract, Fragrance, Ocimum Sanctum Leaf Extract, Saccharomyces Cerevisiae Extract, Curcuma Longa (Turmeric) Root Extract, Corallina Officinalis Extract, Disodium EDTA, 1,2-Hexanediol, Eriobotrya Japonica Leaf Extract, Houttuynia Cordata Extract, Biotin

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 · 22 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
78417-00478417-004-01, 78417-004-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 21 matching rows.

Name, UNII, Kind table
NameUNIIKind
WATER059QF0KO0RIACT
BUTYLENE GLYCOL3XUS85K0RAIACT
ALCOHOL3K9958V90MIACT
C12-14 PARETH-12M0LJS773XWIACT
MENTHOL, UNSPECIFIED FORML7T10EIP3AIACT
ALLANTOIN344S277G0ZIACT
TREHALOSEB8WCK70T7IIACT
PANTHENOLWV9CM0O67ZIACT
ARGININE94ZLA3W45FIACT
AZADIRACHTA INDICA LEAFHKY915780TIACT
AZADIRACHTA INDICA FLOWER3TE8A92UPMIACT
HOLY BASIL LEAFSCJ765569PIACT
SACCHAROMYCES CEREVISIAE978D8U419HIACT
TURMERIC856YO1Z64FIACT
CORALLINA OFFICINALIS4004498D06IACT
EDETATE DISODIUM ANHYDROUS8NLQ36F6MMIACT
1,2-HEXANEDIOLTR046Y3K1GIACT
ERIOBOTRYA JAPONICA LEAFZ02066SV11IACT
HOUTTUYNIA CORDATA FLOWERING TOPRH041UUZ22IACT
BIOTIN6SO6U10H04IACT
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
aff0ecd4-d34e-1672-e053-2a95a90a90eeb44fcd57-7c7d-42d7-97cd-d6a4d48bb0c62020-09-22WarningsExact identifier
spl set id: b44fcd57-7c7d-42d7-97cd-d6a4d48bb0c6

Reported adverse events (FAERS/openFDA)#

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