Label: LANCOME PARIS RENERGIE LIFT MAKEUP BROAD SPECTRUM SPF 27 SUNSCREEN- octinoxate and titanium dioxide liquid

  • NDC Code(s): 49967-335-01, 49967-335-02, 49967-335-03
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 24, 2023

If you are a consumer or patient please visit this version.

  • Active ingredients

    Octinoxate 7.5%

    Titanium dioxide 3.2%

  • Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn
    • if used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin aging caused by the sun
  • Warnings

    For external use only

  • Do not use

    on damaged or broken skin

  • When using this product

    keep out of eyes. Rinse with water to remove.

  • Stop use and ask a doctor if

    rash occurs

  • Keep out of reach of children.

    If swallowed, getmedical help or contact a Poison Control Center right away.

  • Directions

    For sunscreen 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

    protect the product in this container from excessive heat and direct sun

  • Inactive ingredients

    water, cyclopentasiloxane, phenyl trimethicone, cyclohexasiloxane, butylene glycol, propanediol, cetyl PEG/PPG-10/1 dimethicone, pentylene glycol, polyglyceryl-4 isostearate, zea mays (corn) kernel extract, glycine soja (soybean) oil, copernicia cerifera (carnauba) wax, iris florentina root extract, cyhathea medullaris leaf extract; PEG-10 dimethicone, PEG-30 glyceryl stearate, PEG/PPG-18/18 dimethicone, ceramide NP, sorbitol, glycerin, glyceryl caprylate, dimethicone, caffeine, lecithin, sodium levulinate, silylate, cellulose gum, 2-oleamido-1,3-octadecanediol, perlite, aluminum hydroxide, guanosine, magnesium sulfate, cinnamic acid, alcohol denat., poloxamer 188, disodium EDTA, disodium stearoyl glutamate, hydrolyzed linseed extract, hydroxypalmitoyl sphinganine,caprylyl glycol, pentasodium ethylenediamine tetramethylene phosphonate, xanthan gum, levulinic acid, polycaprolactone, BHT, tocopherol, pentaerytrityl tetra-di-t-butyl hydroxyhydrocinnamate, sorbic acid, sodium benzoate, phenoxyethanol; may contain: titanium dioxide, bismuth oxychloride, iron oxides

  • Questions or comments?

    1-800-LANCOME (1-800-526-2663)

    Monday - Friday (9 a.m. - 5 p.m. EST)

  • PRINCIPAL DISPLAY PANEL

    image of a carton

    image of a carton
  • INGREDIENTS AND APPEARANCE
    LANCOME PARIS RENERGIE LIFT MAKEUP BROAD SPECTRUM SPF 27 SUNSCREEN 
    octinoxate and titanium dioxide liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-335
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE32 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    PHENYL TRIMETHICONE (UNII: DR0K5NOJ4R)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 1.5) (UNII: V2W71V8T0X)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    CORN (UNII: 0N8672707O)  
    SOYBEAN OIL (UNII: 241ATL177A)  
    CARNAUBA WAX (UNII: R12CBM0EIZ)  
    IRIS X GERMANICA NOTHOVAR. FLORENTINA ROOT (UNII: M30XO5X4XD)  
    CYATHEA MEDULLARIS LEAF (UNII: G65ROR2RKA)  
    PEG-10 DIMETHICONE (600 CST) (UNII: 8PR7V1SVM0)  
    PEG-30 GLYCERYL STEARATE (UNII: MW8WP96K3D)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    CERAMIDE NP (UNII: 4370DF050B)  
    SORBITOL (UNII: 506T60A25R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CAFFEINE (UNII: 3G6A5W338E)  
    SODIUM LEVULINATE (UNII: VK44E1MQU8)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED FORM (UNII: K679OBS311)  
    9-OCTADECENAMIDE, N-(2-HYDROXY-1-(HYDROXYMETHYL)HEPTADECYL)-, (9Z)- (UNII: 30D478BUNR)  
    PERLITE (UNII: 0SG101ZGK9)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    GUANOSINE (UNII: 12133JR80S)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    CINNAMIC ACID (UNII: U14A832J8D)  
    ALCOHOL (UNII: 3K9958V90M)  
    POLOXAMER 188 (UNII: LQA7B6G8JG)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DISODIUM STEAROYL GLUTAMATE (UNII: 45ASM2L11M)  
    HYDROXYPALMITOYL SPHINGANINE (UNII: NR33W2353T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    LEXIDRONAM PENTASODIUM (UNII: 2ZYX2V82AD)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    LEVULINIC ACID (UNII: RYX5QG61EI)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
    SORBIC ACID (UNII: X045WJ989B)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    MICA (UNII: V8A1AW0880)  
    BISMUTH OXYCHLORIDE (UNII: 4ZR792I587)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-335-011 in 1 CARTON10/30/2019
    130 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49967-335-02110 mL in 1 BOTTLE; Type 0: Not a Combination Product10/30/201912/30/2024
    3NDC:49967-335-031 in 1 CARTON10/30/2019
    310 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/30/2019
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    SICOS ET CIE276993581manufacture(49967-335) , pack(49967-335)
    Establishment
    NameAddressID/FEIBusiness Operations
    BPS 60272259304pack(49967-335)