Label: YVES SAINT LAURENT ALL HOURS FOUNDATION BROAD SPECTRUM SPF 30 SUNSCREEN LUMINOUS MATTE FOUNDATION- octinoxate and titanium dioxide lotion
- NDC Code(s): 49967-270-01, 49967-270-02
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 24, 2023
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- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- Active ingredientS
- Purpose
- Uses
- Warnings
- Flammable until dry.
- Do not use
- When using this product
- Stop use and ask a doctor if
- Keep out of reach of children.
-
Directions
For sunscreen use:
- shake well before use
- apply liberally 15 minutes before sun exposure
- reapply at least every 2 hours
- use a water resistant sunscreen if swimming or sweating
- 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
- children under 6 months of age: Ask a doctor
- Other information
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Inactive ingredients
water, dimethicone, isododecane, alcohol denat., trimethylsiloxysilicate, butylene glycol, PEG-10 dimethicone, synthetic fluorphlogopite, perlite, disteardimonium hectorite, nylon-12, HDI/trimethylol hexyllactone crosspolymer, aluminum hydroxide, isopropyl lauroyl sarcosinate, diisopropyl sebacate, bis-PEG/PPG-14/14 dimethicone,magnesium sulfate, phenoxyethanol, disodium stearoyl glutamate, aluminum hydroxide, dipentaerythrityl tetrahydroxystearate/tetraisostearate, silica silylate, glycerin, tocopherol, caprylic/capric triglyceride, hydrogen dimethicone, silica, BHT, jasminum officinale (jasmine) flower extract, benzyl alcohol, sodium hyaluronate, phenethyl alcohol, linalool, sodium carrageenan, citrus limon (lemon) peel extract, jania rubens extract, fragrance; may contain: iron oxides, titanium dioxide
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
YVES SAINT LAURENT ALL HOURS FOUNDATION BROAD SPECTRUM SPF 30 SUNSCREEN LUMINOUS MATTE FOUNDATION
octinoxate and titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-270 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 67 mg in 1 mL TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE 11 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) ISODODECANE (UNII: A8289P68Y2) ALCOHOL (UNII: 3K9958V90M) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PERLITE (UNII: 0SG101ZGK9) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) NYLON-12 (UNII: 446U8J075B) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) DIPENTAERYTHRITYL TETRAHYDROXYSTEARATE/TETRAISOSTEARATE (UNII: 230K0823CE) GLYCERIN (UNII: PDC6A3C0OX) TOCOPHEROL (UNII: R0ZB2556P8) MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) JASMINUM OFFICINALE FLOWER (UNII: 0Q8K841432) BENZYL ALCOHOL (UNII: LKG8494WBH) HYALURONATE SODIUM (UNII: YSE9PPT4TH) PHENYLETHYL ALCOHOL (UNII: ML9LGA7468) LINALOOL, (+/-)- (UNII: D81QY6I88E) CARRAGEENAN (UNII: 5C69YCD2YJ) LEMON PEEL (UNII: 72O054U628) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-270-01 1 in 1 CARTON 07/25/2022 1 25 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-270-02 4.2 mL in 1 PACKAGE; Type 0: Not a Combination Product 07/25/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/25/2022 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-270) , pack(49967-270) Establishment Name Address ID/FEI Business Operations Socoplan 276221405 pack(49967-270)
