Label: LANCOME PARIS ABSOLUE HAND PREMIUM BX BROAD SPECTRUM SPF 15 SUNSCREEN ABSOLUTE ANTI AGE SPOT UNIFYING AND REPLENISHING TREATMENT- avobenzone, octisalate and octocrylene lotion

  • NDC Code(s): 49967-137-01, 49967-137-02, 49967-137-03, 49967-137-04
  • Packager: L'Oreal USA Products Inc
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 30, 2023

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

  • Active ingredients

    Avobenzone 2%

    Octisalate 5%

    Octocrylene 10%

  • 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:

    ● shake well

    ● apply generously and evenly 15minutes 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, glycerin, alcohol denat., glyceryl stearate, theobroma cacao (cocoa) seed butter, squalane, silica, PEG-100 stearate, glycol distearate, oryza sativa (rice) bran oil, butylene glycol, tocopheryl acetate, lactic acid, vaccinium myrtillus fruit extract, saccharum officinarum (sugar cane) extact, padina pavonica extract, stearic acid, pehnoxyethanol, acer saccharum (sugar maple) extract, palmitic acid, chlorphenesin, polysorbate 80, chlorhexidine digluconate, dimethicone, ammonium polyacryloyldimethyl taurate, dimethiconol, limonene, xanthan gum, linalool, ginkgo biloba leaf extract, dioscorea villosa (wild yam) root extract, propylene glycol, isohexadecane, iron oxides, paraffin, acrylamide/sodium acryloyldimethyltaurate copolymer, rosa centifolia flower extract, tetrasodium EDTA, citrus aurantium dulcis (orange) fruit water, citrus limon (lemon) fruit extract, citronellol, citral, hexyldecanol, glycine soja (soybean) protein, glycyrrhiza glabra (licorice) root extrract, fragrance, sodium benzoate

  • 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 ABSOLUE HAND PREMIUM BX BROAD SPECTRUM SPF 15 SUNSCREEN ABSOLUTE ANTI AGE SPOT UNIFYING AND REPLENISHING TREATMENT 
    avobenzone, octisalate and octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-137
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    ALCOHOL (UNII: 3K9958V90M)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-137-011 in 1 CARTON01/01/200401/01/2004
    1100 g in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:49967-137-021 in 1 CARTON01/01/200401/01/2004
    230 g in 1 BOTTLE; Type 0: Not a Combination Product
    3NDC:49967-137-031 in 1 CARTON01/01/2004
    3100 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:49967-137-041 in 1 CARTON01/01/2004
    430 g in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/01/2004
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-137) , pack(49967-137)