Label: VALENTINO VERY VALENTINO LIGHT LASTING PERFECTING FOUNDATION BROAD SPECTRUM SPF 26 SUNSCREEN- octinoxate and titanium dioxide lotion
- NDC Code(s): 51150-180-01, 51150-180-02, 51150-180-03, 51150-180-04
- Packager: SICOS ET CIE
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 18, 2023
If you are a consumer or patient please visit this version.
- 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.
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Directions
For sunscreen use:
● shake well before use
● apply generously 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, phenyl trimethicone, glycerin, perlite, isopropyl lauroyl sarcosinate, diisopropyl sebacate, disteardimonium hectorite, HDI/trimethylol hexyllactone crosspolymer, bis-PEG/PPG-14/14 dimethicone, magnesium sulfate, phenoxyethanol, disodium stearoyl glutamate, aluminum hydroxide, dipentaerythrityl tetrahydroxystearate/tetraisostearate, hydrogen dimethicone, fragrance, silica silylate, magnesium silicate, silica, linalool, limonene, BHT, citrus aurantium bergamia (bergamot) fruit oil, tin oxide, citronellol, benzyl alcohol; may contain: titanium dioxide, iron oxides, bismuth oxychloride
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
VALENTINO VERY VALENTINO LIGHT LASTING PERFECTING FOUNDATION BROAD SPECTRUM SPF 26 SUNSCREEN
octinoxate and titanium dioxide lotionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:51150-180 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 18 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) DIMETHICONE (UNII: 92RU3N3Y1O) ISODODECANE (UNII: A8289P68Y2) ALCOHOL (UNII: 3K9958V90M) TRIMETHYLSILOXYSILICATE (M/Q 0.8-1.0) (UNII: 25LXE464L2) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R) GLYCERIN (UNII: PDC6A3C0OX) PERLITE (UNII: 0SG101ZGK9) ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) PHENOXYETHANOL (UNII: HIE492ZZ3T) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) DIPENTAERYTHRITYL TETRAHYDROXYSTEARATE/TETRAISOSTEARATE (UNII: 230K0823CE) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) MAGNESIUM SILICATE (UNII: 9B9691B2N9) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) LINALOOL, (+/-)- (UNII: D81QY6I88E) LIMONENE, (+)- (UNII: GFD7C86Q1W) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) BERGAMOT OIL (UNII: 39W1PKE3JI) STANNIC OXIDE (UNII: KM7N50LOS6) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) BENZYL ALCOHOL (UNII: LKG8494WBH) FERRIC OXIDE RED (UNII: 1K09F3G675) BISMUTH OXYCHLORIDE (UNII: 4ZR792I587) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:51150-180-01 1 in 1 CARTON 02/01/2021 1 25 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:51150-180-02 1 mL in 1 PACKET; Type 0: Not a Combination Product 02/01/2021 3 NDC:51150-180-03 1 in 1 CARTON 02/01/2021 3 5 mL in 1 TUBE; Type 0: Not a Combination Product 4 NDC:51150-180-04 0.3 mL in 1 PACKAGE; Type 0: Not a Combination Product 02/01/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 02/01/2021 Labeler - SICOS ET CIE (276993581) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(51150-180) , pack(51150-180) Establishment Name Address ID/FEI Business Operations SOCOPLAN 276221405 pack(51150-180)
