Label: LANCOME PARIS VISIONNAIRE BROAD SPECTRUM SPF 20 SUNSCREEN ADVANCED MULTI CORRECTING ALL SKIN TYPES- avobenzone, octisalate and octocrylene cream

  • NDC Code(s): 49967-194-01, 49967-194-02, 49967-194-03, 49967-194-04, view more
    49967-194-05
  • 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 3%

    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 and evenly 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, glycerin, dimethicone, PTFE, alcohol denat., isopropyl isostearate, behenyl alcohol, synthetic wax, octyldodecanol, C13-14 isoparaffin, yeast extract, tocopheryl acetate, tocopherol, hydrolyzed soy protein, sodium cocoyl glutamate, sodium benzoate, phenoxyethanol, acetyl trifluoromethylphenyl valylglycine, PEG-100 stearate, ethylhexylglycerin, polyacrylamide, calcium PCA, salicyloyl phytosphingosine, ammonium acryloyldimethyltaurate/steareth-25 methacrylate crosspolymer, dimethicone/vinyl dimethicone crosspolymer, dimethiconol, limonene, vinyl dimethicone/methicone silsesquioxane crosspolymer, panthenol, pentaerythrityl tetra-di-t-butyl hydroxyhydrocinnamate, pentylene glycol, linalool, caprylyl glycol, capryloyl salicylic acid, carbomer, disodium stearoyl glutamate, disodium EDTA, cetyl alcohol, methyldihydrojasmonate, cetearyl alcohol, retinyl palmitate, cetearyl glucoside, potassium sorbate, citronellol, BHT, laureth-7, glycine soja (soybean) protein

  • 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 label

    image of a label
  • INGREDIENTS AND APPEARANCE
    LANCOME PARIS VISIONNAIRE BROAD SPECTRUM SPF 20 SUNSCREEN ADVANCED MULTI CORRECTING ALL SKIN TYPES 
    avobenzone, octisalate and octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:49967-194
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE70 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    POLYTETRAFLUOROETHYLENE (UNII: E1NC1JVS3O)  
    ALCOHOL (UNII: 3K9958V90M)  
    ISOPROPYL ISOSTEARATE (UNII: C67IXB9Y7T)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    SYNTHETIC WAX (1200 MW) (UNII: Q3Z4BCH099)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    YEAST, UNSPECIFIED (UNII: 3NY3SM6B8U)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    HYDROLYZED SOY PROTEIN (ENZYMATIC; 2000 MW) (UNII: 1394NXB9L6)  
    SODIUM COCOYL GLUTAMATE (UNII: BMT4RCZ3HG)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ACETYL TRIFLUOROMETHYLPHENYL VALYLGLYCINE, DL- (UNII: 95SP8380V9)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYACRYLAMIDE (10000 MW) (UNII: E2KR9C9V2I)  
    CALCIUM PIDOLATE (UNII: 7Y2LVU5EKK)  
    SALICYLOYL PHYTOSPHINGOSINE (UNII: U891J4JCNH)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)  
    DIMETHICONOL (100000 CST) (UNII: OSA9UP217S)  
    LIMONENE, (+)- (UNII: GFD7C86Q1W)  
    VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER (UNII: 9NH1UDD2RR)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PENTAERYTHRITOL TETRAKIS(3-(3,5-DI-TERT-BUTYL-4-HYDROXYPHENYL)PROPIONATE) (UNII: 255PIF62MS)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CAPRYLOYL SALICYLIC ACID (UNII: 5F7PJF6AA4)  
    CARBOMER HOMOPOLYMER TYPE B (ALLYL SUCROSE CROSSLINKED) (UNII: Z135WT9208)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    METHYL DIHYDROJASMONATE (SYNTHETIC) (UNII: 3GW44CIE3Y)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    .BETA.-CITRONELLOL, (R)- (UNII: P01OUT964K)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    LAURETH-7 (UNII: Z95S6G8201)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:49967-194-011 in 1 CARTON05/01/201706/01/2024
    150 g in 1 JAR; Type 0: Not a Combination Product
    2NDC:49967-194-021 in 1 CARTON05/01/201706/01/2024
    25 g in 1 TUBE; Type 0: Not a Combination Product
    3NDC:49967-194-041 in 1 CARTON12/10/201806/01/2024
    315 g in 1 TUBE; Type 0: Not a Combination Product
    4NDC:49967-194-032 g in 1 PACKET; Type 0: Not a Combination Product05/01/201706/01/2024
    5NDC:49967-194-051 in 1 CARTON05/01/2017
    515 g in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02005/01/2017
    Labeler - L'Oreal USA Products Inc (002136794)
    Establishment
    NameAddressID/FEIBusiness Operations
    L'Oreal USA, Inc.185931458manufacture(49967-194) , pack(49967-194)