NoTS UV PROTECTION SUN

Manufacturer
NoTS Co.,Ltd | Kolmar Korea Co., Ltd.
Effective date
2018-01-08
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
legacy-cache
Hydrated at
2026-08-02 01:05:18

Label at a glance#

ProductNoTS UV PROTECTION SUN
Active ingredientOCTINOXATE, TITANIUM DIOXIDE, ZINC OXIDE, OCTISALATE
Label structure6 sections

Label contents#

Full prescribing information#

ACTIVE INGREDIENT

OTC - ACTIVE INGREDIENT SECTION

Active Ingredient: ETHYLHEXYL METHOXYCINNAMATE 6.8%, TITANIUM DIOXIDE 5.66%, ZINC OXIDE 5.0%, ETHYLHEXYL SALICYLATE 4.5%

INACTIVE INGREDIENT

INACTIVE INGREDIENT SECTION

Inactive Ingredients:

WATER, CYCLOPENTASILOXANE, METHICONE, ALUMINUM HYDROXIDE, STEARIC ACID, DIMETHICONE, DIPROPYLENE GLYCOL, PEG-10 DIMETHICONE, NIACINAMIDE, GLYCERIN, ALUMINUM STEARATE, DICAPRYLYL CARBONATE, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, PORTULACA OLERACEA EXTRACT, BUTYLENE GLYCOL, PHENOXYETHANOL, ETHYLHEXYLGLYCERIN, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, POLYMETHYLSILSESQUIOXANE, BIS-ETHYLHEXYLOXYPHENOL METHOXYPHENYL TRIAZINE, CAPRYLYL GLYCOL, CITRUS GRANDIS (GRAPEFRUIT) PEEL OIL, OLEA EUROPAEA (OLIVE) FRUIT OIL, CITRUS AURANTIFOLIA (LIME) OIL, RIBES NIGRUM (BLACK CURRANT) SEED OIL, ROSE FLOWER OIL, ILLICIUM VERUM (ANISE) FRUIT/SEED OIL, MICROCRYSTALLINE CELLULOSE, CELLULOSE GUM, ALOE BARBADENSIS LEAF EXTRACT, PENTYLENE GLYCOL, 1,2-HEXANEDIOL, PANTHENOL, POLYGLYCERYL-6 POLYRICINOLEATE, LAURUS NOBILIS LEAF EXTRACT, SILICA, POLYURETHANE-11, TOCOPHERYL ACETATE, LAVANDULA ANGUSTIFOLIA (LAVENDER) FLOWER/LEAF/STEM EXTRACT, GLYCERYL CAPRYLATE, ADENOSINE, CAMELLIA SINENSIS LEAF WATER, BENZYL ALCOHOL, DEHYDROACETIC ACID, HAMAMELIS VIRGINIANA (WITCH HAZEL) WATER, ROSA DAMASCENA FLOWER WATER, SODIUM HYALURONATE, ORIGANUM VULGARE LEAF EXTRACT, CHAMAECYPARIS OBTUSA LEAF EXTRACT, SALIX ALBA (WILLOW) BARK EXTRACT, LACTOBACILLUS/SOYBEAN FERMENT EXTRACT, SCUTELLARIA BAICALENSIS ROOT EXTRACT, CINNAMOMUM CASSIA BARK EXTRACT, HIPPOPHAE RHAMNOIDES FRUIT EXTRACT, PHOSPHOLIPIDS, PHYTOSPHINGOSINE, PHYTOSTEROLS, CERAMIDE 3, HIPPOPHAE RHAMNOIDES OIL, TROPOLONE

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-Ray protection

Directions: Dispense appropriate amount on your hand. Spread over your face and other skin area exposed to sun.

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
69716-17069716-170-01

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
0c6f2740-1845-4b7c-8970-5d0f7db5eebfd87a5388-7fa7-44bb-bcff-35d564efd8202020-03-03WarningsExact identifier
spl set id: d87a5388-7fa7-44bb-bcff-35d564efd820

Reported adverse events (FAERS/openFDA)#

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