Label: LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS CLEAR SKIN FACE OIL FREE DRY TOUCH BROAD SPECTRUM SPF 60 SUNSCREEN WATER RESISTANT 80 MINUTES- avobenzone, homosalate, octisalate and octocrylene lotion

  • NDC Code(s): 49967-048-01, 49967-048-02, 49967-048-03, 49967-048-04
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 1, 2024

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  • Active ingredient

    Avobenzone 3%

    Homosalate 15%

    Octisalate 5%

    Octocrylene 7%

  • 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 generously 15 minutes before sun exposure

    ●  reapply:

       ●  after 80 minutes of swimming or sweating

        ●  immediately after towel drying

        ●  at least every 2 hours

    ● 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, silica, dicaprylyl carbonate, styrene/acrylates copolymer, butyloctyl salicylate, methyl methacrylate crosspolymer, nylon-12, PEG-100 stearate, glyceryl stearate, perlite, beeswax, ammonium polyacryloyldimethyl taurate, phenoxyethanol, PEG-8 laurate, behenyl alcohol, sodium stearoyl glutamate, chlorphenesin, p-anisic acid, xanthan gum, tocopherol, disodium EDTA, arachidyl alcohol, diethylhexyl syringylidenemalonate, propylene glycol, cassia alata leaf extract, maltodextrin, stearyl alcohol, t-butyl alcohol, caprylic/capric triglyceride

  • Questions or comments?

    1-888-LRP-LABO 1-888-577-5226

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

  • PRINCIPAL DISPLAY PANEL

    imageof a carton

    imageof a carton
  • INGREDIENTS AND APPEARANCE
    LA ROCHE POSAY LABORATOIRE DERMATOLOGIQUE ANTHELIOS CLEAR SKIN FACE OIL FREE DRY TOUCH BROAD SPECTRUM SPF 60 SUNSCREEN WATER RESISTANT 80 MINUTES 
    avobenzone, homosalate, octisalate and octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-048
    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) HOMOSALATE150 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    NYLON-12 (UNII: 446U8J075B)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    PERLITE (UNII: 0SG101ZGK9)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    P-ANISIC ACID (UNII: 4SB6Y7DMM3)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    DIETHYLHEXYL SYRINGYLIDENEMALONATE (UNII: 3V5U97P248)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    SENNA ALATA LEAF (UNII: 4BXR6YZN92)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    TERT-BUTYL ALCOHOL (UNII: MD83SFE959)  
    CAPRYLIC/CAPRIC/LAURIC TRIGLYCERIDE (UNII: FJ1H6M2JG9)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-048-011 in 1 CARTON01/01/2016
    150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49967-048-023 mL in 1 PACKET; Type 0: Not a Combination Product01/01/2016
    3NDC:49967-048-031 in 1 CARTON01/01/2016
    350 mL in 1 TUBE; Type 0: Not a Combination Product
    4NDC:49967-048-041 in 1 CARTON01/01/2016
    43 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/01/2015
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-048) , pack(49967-048)
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