CELLTRION UV PERFECTION ALWAYS SUN

Manufacturer
Celltrion Skincure Co.,Ltd. | Kolmar Korea Co., Ltd.
Effective date
2018-03-21
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:00:48

Label at a glance#

ProductCELLTRION UV PERFECTION ALWAYS SUN
Active ingredientOCTINOXATE, OCTISALATE, HOMOSALATE, OCTOCRYLENE, TITANIUM DIOXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: ETHYLHEXYL METHOXYCINNAMATE 6.80%, ETHYLHEXYL SALICYLATE 4.50%, HOMOSALATE 3.00%, OCTOCRYLENE 2.50%, TITANIUM DIOXIDE 2.10%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

water, alcohol, C12-15 alkyl benzoate, diethylamino hydroxybenzoyl hexyl benzoate, dipropylene glycol, cyclomethicone, cetyl ethylhexanoate, C20-22 alkyl phosphate, C20-22 alcohols, 1,2-hexanediol, echium plantagineum seed oil, portulaca oleracea extract, centella asiatica extract, houttuynia cordata extract, cardiospermum halicacabum flower/leaf/vine extract, poria cocos sclerotium extract, hippophae rhamnoides fruit extract, helichrysum italicum flower water, glyceryl stearate, behenyl alcohol, aluminum stearate, tromethamine, polyhydroxystearic acid, sodium acrylate/sodium acryloyldimethyl taurate copolymer, propanediol, octyldodecanol, isohexadecane, microcrystalline cellulose, alumina, glyceryl caprylate, niacinamide, polyacrylate crosspolymer-6, xanthan gum, ethylhexylglycerin, hydroxyethyl acrylate/sodium acryloyldimethyl taurate copolymer, polysorbate 80, cellulose gum, sodium hyaluronate, butylene glycol, t-butyl alcohol, helianthus annuus (sunflower) seed oil unsaponifiables, glycerin, tocopherol, fragrance

PURPOSE

OTC - PURPOSE SECTION

Purpose: Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

For external use only

Do not use on damaged or broken skin

When using this product keep out of eyes. Rinse with water to remove.

Stop use and ask a doctor if rash occurs

Replace the cap after use

Keep out of reach of children. if swallowed, get medical help or contact a Poison Control Center right away.

DESCRIPTION

DESCRIPTION SECTION

Uses:

● helps prevent sunburn

● if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun

Directions:

● apply liberally 15 minutes before sun exposure

● reapply at least every 2 hours

● use a water resistant sunscreen if swimming or sweating

● children under 6 months of age: Ask a doctor

● Sun Protection Measures. Spending time in the sun increases your risk of skin cancer and early skin aging. To decrease this risk, regularly use a sunscreen with a Broad Spectrum SPF value of 15 or higher and other sun protection measures including:

● limit time in the sun, especially from 10 a.m.-2 p.m.

● wear long-sleeved shirts, pants, hats, and sunglasses

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-138809448636138GTIN-13: 8809448636138
EAN-13: 8809448636138
GTIN storage (14 digits): 08809448636138
sun carton.jpg

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
47469-48047469-480-01, 47469-480-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 7 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
fec0b38c-8865-4c0a-b36a-f17e3010e54b606e3906-5486-4b49-a6da-e0a112b6ff532018-03-21WarningsExact identifier
spl id: fec0b38c-8865-4c0a-b36a-f17e3010e54b
spl set id: 606e3906-5486-4b49-a6da-e0a112b6ff53

Reported adverse events (FAERS/openFDA)#

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