Dr.Jart Every Sun Day Sunscreen SPF 50

Manufacturer
Have & Be Co., Ltd. | Kolmar Korea Co., Ltd.
Effective date
2016-10-19
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:22:15

Label at a glance#

ProductDr.Jart Every Sun Day Sunscreen SPF 50
Active ingredientZINC OXIDE, OCTINOXATE, OCTISALATE, TITANIUM DIOXIDE
Label structure8 sections

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

ZINC OXIDE 12.660%

OCTINOXATE 6.800%

OCTISALATE 4.500%

TITANIUM DIOXIDE 2.490%

OTC - PURPOSE SECTION

Sunscreen

INDICATIONS & USAGE SECTION

Helps prevent sunburn

If used as directed with other sun protection meausres (see Directions), decreases the risk of skin cancer and early skin aging casued by the sun

DOSAGE & ADMINISTRATION SECTION

Apply liberally 15 minutes before sun exposure.

Use a water resistant sunscreen if swimming or sweating

Reapply at least every 2 hours.

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

Ask a doctor to use for children under 6 months

WARNINGS SECTION

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 using and ask a doctor if rash occurs.

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, Cyclopentasiloxane, Dipropylene Glycol, Dicaprylyl Carbonate, Butyloctyl Salicylate, Peg-10 Dimethicone, Caprylyl Methicone, Glycerin, Disteardimonium Hectorite, Dimethicone, Viscum Album (Mistletoe) Leaf Extract, Centella Asiatica Extract, Portulaca Oleracea Extract, Magnesium Sulfate, Mica, Silica, Phenoxyethanol, Polymethylsilsesquioxane, Aluminum Hydroxide, Triethoxycaprylylsilane, Dimethicone/Vinyl Dimethiconecrosspolymer, Aluminum Stearate, Caprylyl Glycol, Polyglyceryl-6 Polyricinoleate, Vinyl Dimethicone/Methiconesilsesquioxane Crosspolymer, Microcrystalline Cellulose, Glyceryl Caprylate, Lavandula Angustifolia (Lavender) Oil, Iron Oxides, Rose Flower Oil, Polyurethane-11, Juniperus Mexicana Oil, Cellulose Gum, Sodium Hyaluronate, Aminopropyl Dimethicone, Calendula Officinalis Flower, Aloe Barbadensis Leaf Extract

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

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NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
49404-13049404-130-01, 49404-130-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 37 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
9a13a12d-7268-64b9-e053-2995a90a7af7358fe07a-a0c3-4083-9282-78f41723bba72019-12-19WarningsExact identifier
spl set id: 358fe07a-a0c3-4083-9282-78f41723bba7

Reported adverse events (FAERS/openFDA)#

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