APRILSKIN MAGIC SNOW FIXING FOUNDATION 23 NATURAL BEIGE

Manufacturer
APRILSKIN Co., Ltd. | Hankook Cosmetics Manufacturing Co.,Ltd_Eumseong Factory
Effective date
2019-08-13
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 00:15:45

Label at a glance#

ProductAPRILSKIN MAGIC SNOW FIXING FOUNDATION 23 NATURAL BEIGE
Active ingredientTITANIUM DIOXIDE, ADENOSINE, NIACINAMIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Titanium Dioxide, Niacinamide, Adenosine

INACTIVE INGREDIENT SECTION

Camellia Sinensis Leaf Water, Cyclopentasiloxane, Propanediol, Dimethicone, Butylene Glycol, PEG-10 Dimethicone, Dimethicone Crosspolymer, CI 77492, Sodium Chloride, 1,2-Hexanediol, PEG/PPG-18/18 Dimethicone, CI 77491, Triethoxycaprylylsilane, Aluminum Hydroxide, Chlorphenesin, CI 77499, Silica Silylate, Adenosine, Water, Disodium EDTA, Honey, Camellia Japonica Flower Extract, Lentinus Edodes Extract, Malt Extract, Prunus Serrulata Flower Extract, Phenoxyethanol, Ethylhexylglycerin

OTC - PURPOSE SECTION

Skin Protectant - Sun screen, Whitening, Anti-Wrinkle

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

keep out of reach of the children

INDICATIONS & USAGE SECTION

Gently press cushion using a puff and pat evenly on skin. Can be used when applying touch up.

WARNINGS SECTION

1 In the use of the product if the following phenomenon happen, please stop using; if continue using the situation gets worse, please consult with the doctor
1) red, itchy, tingling
2) please stop using if any of the above symptoms appear because of the sun exposure
2 Wounds, eczema, skin inflammation in the face, please do not use
3 Storage precautions
1) seale immediately after using
2) please place in theplace where the infant are unable to access in case eating by mistake
3) avoid placing in high temperature, low temperature or direct sunlight field

DOSAGE & ADMINISTRATION SECTION

for external use only

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

labellabel

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71580-000271580-0002-1

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 5 matching rows.

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
8ffbdaff-9fbb-3930-e053-2a95a90a92b0542c2176-4946-467a-e054-00144ff88e882019-08-13WarningsExact identifier
spl id: 8ffbdaff-9fbb-3930-e053-2a95a90a92b0
spl set id: 542c2176-4946-467a-e054-00144ff88e88

Reported adverse events (FAERS/openFDA)#

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