Label: SUNLEYA AGE MINIMIZING SUN CARE SPF 15- avobenzone, octinoxate, octisalate, oxybenzone cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 30, 2023

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

  • Drug Facts


  • Active ingredients

    Avobenzone 3 % Octinoxate 5 % Octisalate 5 % Oxybenzone 4 %




    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

    • Apply liberally 15 minutes before sun exposure.
    • Reapply at least every 2 hours.
    • Use a water resistant sunscreen if swimming or sweating.
    • Children under 6 months of age: ask a doctor.
    • 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: Sun Protection Measures: 
    • Limit time in the sun especially from 10 am to 2 pm.
    • Wear long-sleeved shirts, pants, hats, and sunglasses.
  • Other information

    Protect the product in this container from excessive heat or direct sun.

  • Inactive ingredients

    water, diisopropyl sebacate, butyrospermum parkii (shea butter), glycerin, cetearyl alcohol, physalis alkekengi calyx extract, arachidyl alcohol, rhodochrosite extract, cucumis sativus (cucumber) fruit extract, stearyl alcohol, styrene/acrylates copolymer, behenyl alcohol, phenoxyethanol, propylene glycol, dimethicone, cetearyl glucoside, arachidyl glucoside, caprylyl glycol, 1,2-hexanediol, tocopheryl acetate, polyacrylamide, ceteareth-33, pentylene glycol, allantoin, thymus mastichina flower oil, c13-14 isoparaffin, peg-8 laurate, sorbic acid, arginine, salvia officinalis (sage) oil, laureth-7, bht, potassium sorbate, linalool, limonene

  • PRINCIPAL DISPLAY PANEL

    SUNLEYA  Age minimizing sun care Sunscreen Cream Broad Spectrum SPF 15  sisley PARIS  NET WT. 1.7 OZ.  50,3 g  CREATIONS HUBERT ISABELLE D'ORNANO   Sisley USA  7 Renaissance Square, 3rd Floor, White Plains, NY 10601  Anti-aging sun care SPF 15.  Face, neck decollete.  Exclusive synergy of active ingredients for a triple anti-aging shield during sun exposure:  Filtration absorbs 90% of UVA-UVB* rays.  Also includes combination of anti-oxidants + DNA cellular protection*. Helps prevent lines, age spots, slackening.  Gives a growing and long lasting tan. *
    in vitro tests

  • Product Labels

    TubeBox 1Box 2

  • INGREDIENTS AND APPEARANCE
    SUNLEYA AGE MINIMIZING SUN CARE   SPF 15
    avobenzone, octinoxate, octisalate, oxybenzone cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66097-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    OCTINOXATE (UNII: 4Y5P7MUD51) (OCTINOXATE - UNII:4Y5P7MUD51) OCTINOXATE50 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE40 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    DIISOPROPYL SEBACATE (UNII: J8T3X564IH)  
    SHEANUT OIL (UNII: O88E196QRF)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    PHYSALIS ALKEKENGI CALYX (UNII: AL7F9NO9HR)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    MANGANESE CARBONATE (UNII: 9ZV57512ZM)  
    CUCUMBER (UNII: YY7C30VXJT)  
    STEARYL ALCOHOL (UNII: 2KR89I4H1Y)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CETEARETH-33 (UNII: R42C2O714B)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    ALLANTOIN (UNII: 344S277G0Z)  
    THYMUS MASTICHINA FLOWERING TOP OIL (UNII: 9NP0832457)  
    C13-14 ISOPARAFFIN (UNII: E4F12ROE70)  
    PEG-8 LAURATE (UNII: 762O8IWA10)  
    SORBIC ACID (UNII: X045WJ989B)  
    ARGININE (UNII: 94ZLA3W45F)  
    SAGE OIL (UNII: U27K0H1H2O)  
    EDETATE SODIUM (UNII: MP1J8420LU)  
    LAURETH-7 (UNII: Z95S6G8201)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    LINALOOL, (+/-)- (UNII: D81QY6I88E)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66097-002-501 in 1 BOX01/21/2013
    150.3 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/21/2013
    Labeler - C.F.E.B. Sisley (262279246)