Label: LANCOME PARIS TEINT IDOLE ULTRA CARE AND GLOW SKINCARE FOUNDATION BROAD SPECTRUM SPF 27 SUNSCREEN- ensulizole liquid
- NDC Code(s): 49967-676-01, 49967-676-02, 49967-676-03, 49967-676-04
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated June 25, 2024
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- Official Label (Printer Friendly)
- Active ingredient
- 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
● 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
dimethicone, water, isododecane, alcohol denat., trimethylsiloxysilicate, propylene glycol, glycerin, PEG/PPG-18/18 dimethicone, silica, synthetic fluorphlogopite, polysilicone-11, rosa gallica flower extract, moringa oleifera seed extract, polymnia sonchifolia root juice, sorbitol, mandelic acid, PEG-10 dimethicone, alpha-glucan oligosaccharide. sodium chloride, sodium hyaluronate, sodium hydroxide, silica silylate, cellulose acetate butyrate, aluminum hydroxide, ammonium polyacryloyldimethyl taurate, disodium phosphate, disodium stearoyl glutamate, hydroxyethylpiperazine ethane sulfonic acid, caprylyl glycol, citric acid, lactobacillus, maltodextrin, polyphosphorylcholine glycol acrylate, polyvinyl alcohol, butylene glycol, tocopherol, phenoxyethanol, fragrance, linalool, geraniol, limonene, citral, citronellol, benzyl alcohol; may contain: titanium dioxide, iron oxides
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- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LANCOME PARIS TEINT IDOLE ULTRA CARE AND GLOW SKINCARE FOUNDATION BROAD SPECTRUM SPF 27 SUNSCREEN
ensulizole liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-676 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ENSULIZOLE (UNII: 9YQ9DI1W42) (ENSULIZOLE - UNII:9YQ9DI1W42) ENSULIZOLE 36 mg in 1 mL Inactive Ingredients Ingredient Name Strength DIMETHICONE (UNII: 92RU3N3Y1O) WATER (UNII: 059QF0KO0R) ISODODECANE (UNII: A8289P68Y2) ALCOHOL (UNII: 3K9958V90M) TRIMETHYLSILOXYSILICATE (M/Q 0.6-0.8) (UNII: 5041RX63GN) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) GLYCERIN (UNII: PDC6A3C0OX) PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5) ROSA GALLICA FLOWER (UNII: X8W61WUV70) SORBITOL (UNII: 506T60A25R) MANDELIC ACID (UNII: NH496X0UJX) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) SODIUM CHLORIDE (UNII: 451W47IQ8X) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SODIUM HYDROXIDE (UNII: 55X04QC32I) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) AMMONIUM POLYACRYLOYLDIMETHYL TAURATE (55000 MPA.S) (UNII: F01RIY4371) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) HYDROXYETHYLPIPERAZINE ETHANE SULFONIC ACID (UNII: RWW266YE9I) CAPRYLYL GLYCOL (UNII: 00YIU5438U) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) MALTODEXTRIN (UNII: 7CVR7L4A2D) POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) TOCOPHEROL (UNII: R0ZB2556P8) PHENOXYETHANOL (UNII: HIE492ZZ3T) LINALOOL, (+/-)- (UNII: D81QY6I88E) GERANIOL (UNII: L837108USY) LIMONENE, (+)- (UNII: GFD7C86Q1W) CITRAL (UNII: T7EU0O9VPP) .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K) BENZYL ALCOHOL (UNII: LKG8494WBH) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-676-01 1 in 1 CARTON 05/01/2022 05/01/2022 1 30 mL in 1 TUBE; Type 0: Not a Combination Product 2 NDC:49967-676-02 1 mL in 1 PACKET; Type 0: Not a Combination Product 05/01/2022 12/08/2026 3 NDC:49967-676-03 1.6 mL in 1 PACKAGE; Type 0: Not a Combination Product 05/01/2022 01/19/2026 4 NDC:49967-676-04 1 in 1 CARTON 05/01/2022 05/16/2027 4 30 mL in 1 BOTTLE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 05/01/2022 05/16/2027 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-676) , pack(49967-676) Establishment Name Address ID/FEI Business Operations SOCOPLAN 276221405 pack(49967-676)
