Label: LANCOME PARIS ABSOLUE MAKEUP BROAD SPECTRUM SPF 20 SUNSCREEN ABSOLUTE REPLENISHING MAKEUP FOR DRY AND VERY DRY SKIN- octinoxate cream

  • NDC Code(s): 49967-596-01, 49967-596-02
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated June 28, 2024

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  • Active ingredient

    Octinoxate 7.5%

  • 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, get medical 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, cyclohexasiloxane, hydrogenated polyisobutene, glycerin, cyclopentasiloxane, polyglyceryl-4 isostearate, petrolatum, nylon-12, cetyl PEG/PPG-10/1 dimethicone, hexyl laurate, disteardimonium hectorite, pentylene glycol, C18-36 acid glycol ester, linalool, paraffin, glycyrrhiza glabra (licorice) extract, diphenyl dimethicone, padina pavonica extract, cellulose gum, aluminum hydroxide, magnesium sulfate, limonene, disodium stearoyl glutamate, tristearin, dioscorea villosa (wild yam) root extract, acrylates copolymer, hexyldecanol, fragrance, methylparaben, phenoxyethanol, butylparaben, diazolidinyl urea, tocopherol; may contain: mica, titanium dioxide, iron oxides

  • Questions or comments?

    1-800-LANCOME (1800-526-2663) Monday - Friday (9 a.m. - 5 p.m. EST)

  • PRINCIPAL DISPLAY PANEL

    image of a labelimage of a label

  • INGREDIENTS AND APPEARANCE
    LANCOME PARIS ABSOLUE MAKEUP BROAD SPECTRUM SPF 20 SUNSCREEN ABSOLUTE REPLENISHING MAKEUP FOR DRY AND VERY DRY SKIN 
    octinoxate cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-596
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE75 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    HYDROGENATED POLYISOBUTENE (450 MW) (UNII: 7YR4ZFS62E)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    polyglyceryl-4 isostearate (UNII: 820DPX33S7)  
    petrolatum (UNII: 4T6H12BN9U)  
    nylon-12 (UNII: 446U8J075B)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 4) (UNII: 8INO2K35FA)  
    hexyl laurate (UNII: 4CG9F9W01Q)  
    disteardimonium hectorite (UNII: X687XDK09L)  
    pentylene glycol (UNII: 50C1307PZG)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Paraffin (UNII: I9O0E3H2ZE)  
    DIPHENYL DIMETHICONE (300 CST) (UNII: ZF5SBB12ZZ)  
    PADINA PAVONICA (UNII: 177U06NHZI)  
    CARBOXYMETHYLCELLULOSE SODIUM, UNSPECIFIED (UNII: K679OBS311)  
    aluminum hydroxide (UNII: 5QB0T2IUN0)  
    MAGNESIUM SULFATE, UNSPECIFIED FORM (UNII: DE08037SAB)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    disodium stearoyl glutamate (UNII: 45ASM2L11M)  
    tristearin (UNII: P6OCJ2551R)  
    DIOSCOREA VILLOSA TUBER (UNII: IWY3IWX2G8)  
    LUVISET 360 (UNII: 05BG6GY6YK)  
    hexyldecanol (UNII: 151Z7P1317)  
    methylparaben (UNII: A2I8C7HI9T)  
    phenoxyethanol (UNII: HIE492ZZ3T)  
    butylparaben (UNII: 3QPI1U3FV8)  
    diazolidinyl urea (UNII: H5RIZ3MPW4)  
    tocopherol (UNII: R0ZB2556P8)  
    mica (UNII: V8A1AW0880)  
    titanium dioxide (UNII: 15FIX9V2JP)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-596-011 in 1 CARTON11/01/2007
    135 mL in 1 JAR; Type 0: Not a Combination Product
    2NDC:49967-596-0210 mL in 1 JAR; Type 0: Not a Combination Product11/01/2007
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/01/2007
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-596)
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