CELLTRION LXTR WATER CUSHION No 21 PINK BEIGE

Manufacturer
Celltrion Skincure Co.,Ltd. | Kolmar Korea Co., Ltd.
Effective date
2018-03-21
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-02 01:00:48

Label at a glance#

ProductCELLTRION LXTR WATER CUSHION No 21 PINK BEIGE
Active ingredientTITANIUM DIOXIDE, OCTINOXATE, OCTISALATE, ZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active ingredients: TITANIUM DIOXIDE 7.68%, ETHYLHEXYL METHOXYCINNAMATE 7.00%, ETHYLHEXYL SALICYLATE 4.00%, ZINC OXIDE 2.94%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive ingredients:

water, propanediol, diphenylsiloxy phenyl trimethicone, cyclopentasiloxane, cetyl PEG/PPG-10/1 dimethicone, diethylamino hydroxybenzoyl hexyl benzoate, butylene glycol dicaprylate/dicaprate, bis-ethylhexyloxyphenol methoxyphenyl triazine, sodium chloride, disteardimonium hectorite, diisostearyl malate, cyclohexasiloxane, polymethyl methacrylate, gynostemma pentaphyllum extract, fragrance, dimethicone, glyceryl behenate/eicosadioate, sorbitan sesquioleate, allantoin, PEG-30 dipolyhydroxystearate, triethoxycaprylylsilane, triethyl citrate, aluminum hydroxide, acrylates/ethylhexyl acrylate/dimethicone methacrylate copolymer, dimethicone/vinyl dimethicone crosspolymer, 1,2-hexanediol, disodium EDTA, biosaccharide gum-1, mica, glycerin, butylene glycol, barium sulfate, nacre powder, diamond powder, sapphire powder, amethyst powder, hydrogen dimethicone, vinyl dimethicone, ethylhexylglycerin, limnanthes alba (meadowfoam) seed oil, rosa ambassador/rosa peace phytoplacenta extract, sodium hyaluronate, asparagus officinalis stem extract, gluconolactone, undaria pinnatifida extract, calcium gluconate, hydrolyzed sodium hyaluronate, lecithin, polysorbate 20, alcohol, sh-oligopeptide-1, dipotassium phosphate, sodium ascorbyl phosphate, oligopeptide-2, oligopeptide-4, tromethamine, potassium phosphate, hydrochloric acid, iron oxides(CI 77492), iron oxides(CI 77491), iron oxides(CI 77499)

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

Products#

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
47469-49047469-490-01, 47469-490-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 6 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
07dfd663-ee1c-4a7e-831e-d826fa764a1337d13e86-59e3-4607-b857-54cd328cb5c32018-03-21WarningsExact identifier
spl id: 07dfd663-ee1c-4a7e-831e-d826fa764a13
spl set id: 37d13e86-59e3-4607-b857-54cd328cb5c3

Reported adverse events (FAERS/openFDA)#

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