Label: DAYWEAR ANTI OXIDANT 72H-HYDRATION SORBET CREME BROAD SPECTRUM SPF 15- avobenzone, homosalate, octisalate, and octocrylene cream

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

Drug Label Information

Updated November 21, 2023

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Avobenzone 2.0%Sunscreen
    Homosalate 4.0%Sunscreen
    Octisalate 4.5%Sunscreen
    Octocrylene 2.0%Sunscreen
  • Use

    • helps prevent sunburn
  • 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 product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    For sunscreen use:

    • apply liberally and evenly 15 minutes before sun exposure
    • reapply at least every two 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
  • Inactive ingredients

    water\aqua\eau•glycerin•alcohol denat.•pentylene glycol•caprylyl methicone•biosaccharide gum-1•ammonium acryloyldimethyltaurate/vp copolymer•cucumis sativus (cucumber) fruit extract•sodium hyaluronate•thermus thermophillus ferment•ethylbisiminomethylguaiacol manganese chloride•ergothioneine•tocopheryl acetate•tetrahexyldecyl ascorbate•cyclodextrin•psidium guajava (guava) fruit extract•caffeine•narcissus tazetta bulb extract•polygonum cuspidatum root extract•algae extract•helianthus annuus (sunflower) seed extract•vitis vinifera (grape) seed extract•triticum vulgare (wheat) germ extract•hordeum vulgare (barley) extract\extrait d'orge•gentiana lutea (gentian) root extract•linoleic acid•cholesterol•glycyrrhetinic acid•saccharomyces lysate extract•palmitoyl hydroxypropyltrimonium amylopectin/glycerin crosspolymer•artemia extract•propylene glycol dicaprate•ethylhexylglycerin•tocopherol•propanediol•squalane•glucose•acrylates/c10-30 alkyl acrylate crosspolymer•butylene glycol•lecithin•citric acid•sodium hydroxide•fragrance (parfum)•disodium edta•bht•sodium benzoate•phenoxyethanol•blue 1 (ci 42090) <iln48747>

  • Other information

    protect the product in this container from excessive heat and direct sun

  • PRINCIPAL DISPLAY PANEL - 50 ml Jar Carton

    ESTĒE LAUDER

    DayWear
    Anti-Oxidant 72H-Hydration Sorbet Creme
    Broad Spectrum SPF 15

    Normal/Combination Skin

    POIDS NET WT. 1.7 OZ./50 ml e

    PRINCIPAL DISPLAY PANEL - 50 ml Jar Carton
  • INGREDIENTS AND APPEARANCE
    DAYWEAR ANTI OXIDANT 72H-HYDRATION SORBET CREME BROAD SPECTRUM SPF 15 
    avobenzone, homosalate, octisalate, and octocrylene cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11559-055
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE40 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE45 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE20 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    BIOSACCHARIDE GUM-1 (UNII: BB4PU4V09H)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE/VP COPOLYMER (UNII: W59H9296ZG)  
    CUCUMBER (UNII: YY7C30VXJT)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    THERMUS THERMOPHILUS LYSATE (UNII: 775R692494)  
    ETHYLBISIMINOMETHYLGUAIACOL MANGANESE CHLORIDE (UNII: SM5YJ88LTU)  
    ERGOTHIONEINE (UNII: BDZ3DQM98W)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    GUAVA (UNII: 74O70D6VG0)  
    CAFFEINE (UNII: 3G6A5W338E)  
    HELIANTHUS ANNUUS SEEDCAKE (UNII: 482WYF7XLC)  
    GRAPE (UNII: 6X543N684K)  
    WHEAT (UNII: 4J2I0SN84Y)  
    BARLEY (UNII: 5PWM7YLI7R)  
    LINOLEIC ACID (UNII: 9KJL21T0QJ)  
    CHOLESTEROL (UNII: 97C5T2UQ7J)  
    ENOXOLONE (UNII: P540XA09DR)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SQUALANE (UNII: GW89575KF9)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    SODIUM HYDROXIDE (UNII: 55X04QC32I)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    SODIUM BENZOATE (UNII: OJ245FE5EU)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    CARBOMER INTERPOLYMER TYPE A (ALLYL SUCROSE CROSSLINKED) (UNII: 59TL3WG5CO)  
    GLUCOSE 1,6-BISPHOSPHATE (UNII: DRX17R6AM2)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    BRINE SHRIMP (UNII: 3ID50N77DH)  
    TRIMETHYLPENTANEDIOL/ADIPIC ACID/GLYCERIN CROSSPOLYMER (25000 MPA.S) (UNII: 587WKM3S9Q)  
    SACCHAROMYCES LYSATE (UNII: R85W246Z1C)  
    GENTIANA LUTEA ROOT (UNII: S72O3284MS)  
    AGAR, UNSPECIFIED (UNII: 89T13OHQ2B)  
    REYNOUTRIA JAPONICA ROOT (UNII: 7TRV45YZF7)  
    NARCISSUS TAZETTA BULB (UNII: K17762966S)  
    .BETA.-CYCLODEXTRIN SULFOBUTYL ETHER (UNII: H1HJ8WR7WG)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:11559-055-011 in 1 CARTON12/01/2018
    150 mL in 1 JAR; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/01/2018
    Labeler - ESTEE LAUDER INC (005914387)
    Registrant - Estee Lauder Companies Inc. (790802086)
    Establishment
    NameAddressID/FEIBusiness Operations
    Whitman Laboratories Ltd.216866277manufacture(11559-055) , pack(11559-055) , label(11559-055)