NOTS Once Finishing

Manufacturer
NoTS Co.,Ltd | Kolmar Korea Co., Ltd.
Effective date
2018-03-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
legacy-cache
Hydrated at
2026-08-02 01:00:31

Label at a glance#

ProductNOTS Once Finishing
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, OCTISALATE, ZINC OXIDE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient : ETHYLHEXYL METHOXYCINNAMATE 6%, TITANIUM DIOXIDE 4.02%, ETHYLHEXYL SALICYLATE 2%, ZINC OXIDE 1.92%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

INACTIVE INGREDIENT:

WATER, CYCLOPENTASILOXANE, PROPYLENE GLYCOL, BUTYLENE GLYCOL, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, ISODODECANE, ISOEICOSANE, ISOHEXADECANE, CAPRYLYL METHICONE, PEG-10 DIMETHICONE, TALC, METHICONE, CYCLOMETHICONE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, NIACINAMIDE, ALUMINUM HYDROXIDE, ALUMINUM STEARATE, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, DISTEARDIMONIUM HECTORITE, DIMETHICONE, MAGNESIUM SULFATE, BETAINE, C12-14 PARETH-3, PALMITIC ACID, CHROMIUM OXIDE GREENS, OCTYLDODECANOL, ECHIUM PLANTAGINEUM SEED OIL, CARDIOSPERMUM HALICACABUM FLOWER/LEAF/VINE EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL UNSAPONIFIABLES, TOCOPHEROL, TOCOPHERYL ACETATE, CITRUS MEDICA LIMONUM (LEMON) PEEL OIL, CITRUS AURANTIUM BERGAMIA (BERGAMOT) FRUIT OIL, CITRUS AURANTIFOLIA (LIME) OIL, CITRUS AURANTIUM DULCIS (ORANGE) PEEL OIL, PINUS SYLVESTRIS LEAF OIL, EUCALYPTUS GLOBULUS LEAF OIL, ADENOSINE, LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL, ULTRAMARINES, ARGANIA SPINOSA KERNEL OIL, OLEA EUROPAEA (OLIVE) FRUIT OIL, ROSA DAMASCENA FLOWER WATER, BENZYL ALCOHOL, DEHYDROACETIC ACID, CALENDULA OFFICINALIS FLOWER EXTRACT, GLYCERIN, SAMBUCUS NIGRA FLOWER EXTRACT, PALMITOYL HEXAPEPTIDE-12, CERAMIDE 3, ROSMARINUS OFFICINALIS (ROSEMARY) LEAF EXTRACT, HEDERA HELIX (IVY) EXTRACT, ALLIUM SATIVUM (GARLIC) BULB EXTRACT, PINUS PALUSTRIS LEAF EXTRACT, LAMIUM ALBUM FLOWER EXTRACT, ARNICA MONTANA FLOWER EXTRACT, ARCTIUM MAJUS ROOT EXTRACT, NASTURTIUM OFFICINALE EXTRACT, CHAMOMILLA RECUTITA (MATRICARIA) FLOWER EXTRACT, METHYLPARABEN, BUTYLPARABEN, ETHYLPARABEN, PROPYLPARABEN, ISOBUTYLPARABEN, CAMELLIA SINENSIS LEAF EXTRACT, SODIUM HYALURONATE, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER EXTRACT, PORTULACA OLERACEA EXTRACT, CHAMAECYPARIS OBTUSA LEAF EXTRACT, SALIX ALBA (WILLOW) BARK EXTRACT, ORIGANUM VULGARE LEAF EXTRACT, SCUTELLARIA BAICALENSIS ROOT EXTRACT, CINNAMOMUM CASSIA BARK EXTRACT, LACTOBACILLUS/SOYBEAN FERMENT EXTRACT, ACETYLPHYTOSPHINGOSINE, SAUSSUREA INVOLUCRATA EXTRACT, LILIUM CANDIDUM FLOWER EXTRACT, CHRYSANTHEMUM INDICUM FLOWER EXTRACT, ALCOHOL, SODIUM HYDROXIDE

PURPOSE

OTC - PURPOSE SECTION

Purpose : Sunscreen

WARNINGS

WARNINGS SECTION

Warnings:

Stop use and ask dermatologist or doctor

   if signs of redness, skin swelling, itchy spots, irritation or rash and other appear

   the above signs appear in the applied area by direct rays of the sun

Do not use over - wounds - rashes - inflammations - other troubled areas.

Do not stay too long in the sun, even while using a sunscreen product.

When using - Avoid the eye area - Must close the cap after using

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

DESCRIPTION

DESCRIPTION SECTION

Uses:

- UV Protection

- Helps Prevent Sunburn

Directions:

With appropriate amount, use your fingers to gently spread evenly on your face to even out the texture prior to makeup.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Image of cartonImage of carton

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
69716-32069716-320-01, 69716-320-02

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
43c2bffe-ccbf-4565-9ed4-ea552a6085a6dff0e6dd-4b4c-4dab-a135-d1836b82c6ce2019-12-03WarningsExact identifier
spl set id: dff0e6dd-4b4c-4dab-a135-d1836b82c6ce

Reported adverse events (FAERS/openFDA)#

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