Label: LANCOME PARIS TEINT IDOLE ULTRA WEAR BREATHABLE COVERAGE FOUNDATION BROAD SPECTRUM SPF 25 SUNSCREEN- octinoxate and titanium dioxide liquid
- NDC Code(s): 49967-302-01, 49967-302-02, 49967-302-03, 49967-302-04
- Packager: L'Oreal USA Products Inc
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated December 19, 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.
-
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
-
Inactive ingredients
water, dimethicone, isododecane, alcohol denat., trimethylsiloxysilicate, butylene glycol, PEG-10 dimethicone, perlite, synthetic fluorphlogopite, moringa oleifera seed extract, polymnia sonchifolia root juice, calcium aluminum borosilicate, glycerin, dipentaerythrityl tetrahydroxystearate/tetraisostearate, alpha-glucan oligosaccharide, sodium hyaluronate, silica, silica silylate, HDI/trimethylol hexyllactone crosspolymer, cellulose, aluminum hydroxide, magnesium sulfate, nylon-12, disodium phosphate, disodium stearoyl glutamate, isopropyl lauroyl sarcosinate, hydrogen dimethicone, citric acid, diisopropyl sebacate, bis-PEG/PPG-14/14 dimethicone, lactobacillus, maltodextrin, disteardimonium hectorite, BHT, tocopherol, phenoxyethanol; may contain: titanium dioxide, iron oxides
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
LANCOME PARIS TEINT IDOLE ULTRA WEAR BREATHABLE COVERAGE FOUNDATION BROAD SPECTRUM SPF 25 SUNSCREEN
octinoxate and titanium dioxide liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-302 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 51 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) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) PERLITE (UNII: 0SG101ZGK9) MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M) MORINGA OLEIFERA SEED (UNII: TIX5482832) SMALLANTHUS SONCHIFOLIUS ROOT JUICE (UNII: M9S7HX36CT) CALCIUM ALUMINUM BOROSILICATE (UNII: 3JRB8A35M0) GLYCERIN (UNII: PDC6A3C0OX) DIPENTAERYTHRITYL TETRAHYDROXYSTEARATE/TETRAISOSTEARATE (UNII: 230K0823CE) .ALPHA.-GLUCAN OLIGOSACCHARIDE (UNII: S95658MI3W) HYALURONATE SODIUM (UNII: YSE9PPT4TH) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) HEXAMETHYLENE DIISOCYANATE/TRIMETHYLOL HEXYLLACTONE CROSSPOLYMER (UNII: WB5K9Y35Y9) POWDERED CELLULOSE (UNII: SMD1X3XO9M) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) NYLON-12 (UNII: 446U8J075B) SODIUM PHOSPHATE, DIBASIC, ANHYDROUS (UNII: 22ADO53M6F) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) ISOPROPYL LAUROYL SARCOSINATE (UNII: LYR06W430J) HYDROGEN DIMETHICONE (13 CST) (UNII: 4QGR4P2YOI) CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP) DIISOPROPYL SEBACATE (UNII: J8T3X564IH) BIS-PEG/PPG-14/14 DIMETHICONE (UNII: X2I70H0QJE) EMMENTAL LACTOBACILLUS (UNII: B253LSV04X) MALTODEXTRIN (UNII: 7CVR7L4A2D) DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L) BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K) TOCOPHEROL (UNII: R0ZB2556P8) PHENOXYETHANOL (UNII: HIE492ZZ3T) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-302-01 1 in 1 CARTON 12/12/2022 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-302-02 100 mL in 1 TUBE; Type 0: Not a Combination Product 12/12/2022 3 NDC:49967-302-03 1 mL in 1 PACKET; Type 0: Not a Combination Product 12/12/2022 4 NDC:49967-302-04 0.4 mL in 1 PACKAGE; Type 0: Not a Combination Product 12/12/2022 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 12/12/2022 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-302) , pack(49967-302) Establishment Name Address ID/FEI Business Operations BPS60 272259304 pack(49967-302) Establishment Name Address ID/FEI Business Operations Socoplan 276221405 pack(49967-302)
