Label: GARNIER OMBRELLE ULTRA LIGHT ADVANCED 30- avobenzone, homosalate, octisalate, octocrylene and oxybenzone/ lotion

  • NDC Code(s): 49967-656-01
  • Packager: L'OREAL USA PRODUCTS INC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Export only

Drug Label Information

Updated January 31, 2024

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  • Active ingredients

    Avobenzone 3%

    Homosalate 10%

    Octisalate 5%

    Octocrylene 5%

    Oxbenzone 3%

  • Warnings

    For external use only. When using this product avoid contact with eyes. If contact occurs, rinse thoroughlly with water. Do not use on broken skin. 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 

    Adults and children over 6 months and up. Apply generously and evenly 15 minutes before sun exposure. Reapply at least every 2 hours, use a water resistant sunscreen if swimming or sweating.

  • Inactive ingredients

    water, cyclopentasiloxane, dicaprylyl ether, alcohol denat., silica, dimethicone, styrene/acrylates copolymer, PEG-30 dipolyhydroxystearate, cyclohexasiloxane, polymethylsilsesquioxane, nylon-12, dicaprylyl carbonate, phenoxyethanol, lauryl PEG/PPG-18/18 methicone, sodium chloride, caprylyl glycol, PEG-8 laurate, methylparaben, poly c10-30 alkyl acrylate, disteardimonium hectorite, isostearyl alcohol. disodium EDTA, dodecane, poloxamer 407, tocopherol, sodium dodecylbenzenesulfonate

  • PRINCIPAL DISPLAY PANEL

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  • INGREDIENTS AND APPEARANCE
    GARNIER OMBRELLE ULTRA LIGHT ADVANCED 30 
    avobenzone, homosalate, octisalate, octocrylene and oxybenzone/ lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-656
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE50 mg  in 1 mL
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DICAPRYLYL ETHER (UNII: 77JZM5516Z)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    PEG-30 DIPOLYHYDROXYSTEARATE (UNII: 9713Q0S7FO)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CYCLOMETHICONE 6 (UNII: XHK3U310BA)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    NYLON-12 (UNII: 446U8J075B)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    LAURYL PEG/PPG-18/18 METHICONE (UNII: ZJ5S27D9NX)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    ISOSTEARYL ALCOHOL (UNII: Q613OCQ44Y)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    DODECENE (UNII: WYE669F3GR)  
    POLOXAMER 407 (UNII: TUF2IVW3M2)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    SODIUM DODECYLBENZENESULFONATE (UNII: 554127163Y)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-656-011 in 1 CARTON02/01/201510/30/2024
    150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    export only02/01/201510/30/2024
    Labeler - L'OREAL USA PRODUCTS INC (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'OREAL USA, INC624244349manufacture(49967-656) , pack(49967-656)
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