Label: LANCOME PARIS TEINT IDOLE ULTRA 24H MAKEUP BROAD SPECTRUM SPF 15 SUNSCREEN- octinoxate liquid
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NDC Code(s):
49967-956-01,
49967-956-02,
49967-956-03,
49967-956-04, view more49967-956-05, 49967-956-06, 49967-956-07
- 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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- 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.
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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
water, cyclohexasiloxane, alcohol denat., isododecane, butylene glycol, acrylates/polytrimethylsiloxymethacrylate copolymer, nylon-12, PEG-10 dimethicone, isohexadecane, silica, perlite, aluminum hydroxide, magnesium sulfate, disodium stearoyl glutamate, cetyl PEG/PPG-10/1 dimethicone; may contain: titanium dioxide, iron oxides
- Questions or comments?
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
LANCOME PARIS TEINT IDOLE ULTRA 24H MAKEUP BROAD SPECTRUM SPF 15 SUNSCREEN
octinoxate liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:49967-956 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE 30 mg in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) CYCLOMETHICONE 6 (UNII: XHK3U310BA) ALCOHOL (UNII: 3K9958V90M) ISODODECANE (UNII: A8289P68Y2) BUTYLENE GLYCOL (UNII: 3XUS85K0RA) NYLON-12 (UNII: 446U8J075B) PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0) ISOHEXADECANE (UNII: 918X1OUF1E) SILICON DIOXIDE (UNII: ETJ7Z6XBU4) PERLITE (UNII: 0SG101ZGK9) ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0) MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB) DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M) CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP) TITANIUM DIOXIDE (UNII: 15FIX9V2JP) FERRIC OXIDE RED (UNII: 1K09F3G675) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:49967-956-01 1 in 1 CARTON 07/01/2016 1 30 mL in 1 BOTTLE; Type 0: Not a Combination Product 2 NDC:49967-956-02 1 in 1 CARTON 07/01/2016 2 10 mL in 1 BOTTLE; Type 0: Not a Combination Product 3 NDC:49967-956-03 1 in 1 CARTON 07/01/2016 12/30/2024 3 5 mL in 1 BOTTLE; Type 0: Not a Combination Product 4 NDC:49967-956-04 110 mL in 1 BOTTLE; Type 0: Not a Combination Product 07/01/2016 12/30/2024 5 NDC:49967-956-05 1.6 mL in 1 PACKET; Type 0: Not a Combination Product 07/01/2016 12/30/2024 6 NDC:49967-956-06 1 in 1 CARTON 06/01/2019 12/30/2024 6 15 mL in 1 BOTTLE; Type 0: Not a Combination Product 7 NDC:49967-956-07 0.3 mL in 1 CONTAINER; Type 0: Not a Combination Product 08/01/2020 12/30/2024 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M020 07/01/2016 Labeler - L'Oreal USA Products Inc (002136794) Establishment Name Address ID/FEI Business Operations SICOS ET CIE 276993581 manufacture(49967-956) , pack(49967-956)
