Label: ETUDE SUNPRISE MILD AIRY FINISH SUNSTICK- avobenzone, homosalate, octisalate, octocrylene stick

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

Drug Label Information

Updated February 17, 2025

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  • Route of administration

    TOPICAL

  • 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 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.
  • Inactive ingredients

    METHYL METHACRYLATE CROSSPOLYMER, DIETHYLHEXYL CARBONATE, SYNTHETIC WAX, DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER, ISOPROPYL PALMITATE, DIPHENYLSILOXY PHENYL TRIMETHICONE, BUTYLOCTYL SALICYLATE, DIISOSTEARYL MALATE, DIMETHICONE, PHENETHYL BENZOATE, DIMETHICONOL, TRISILOXANE, ETHYLHEXYL ISONONANOATE, PHENYL PROPYL TRIMETHICONE, SYNTHETIC FLUORPHLOGOPITE, POLYETHYLENE, BIS-BEHENYL/ISOSTEARYL/PHYTOSTERYL DIMER DILINOLEYL DIMER DILINOLEATE, ETHYLENE/PROPYLENE COPOLYMER, CAMELLIA JAPONICA SEED OIL, SILICA DIMETHYL SILYLATE, CANDELILLA WAX ESTERS, VINYL DIMETHICONE/METHICONE SILSESQUIOXANE CROSSPOLYMER, COPERNICIA CERIFERA (CARNAUBA) WAX, PHYLLANTHUS EMBLICA FRUIT EXTRACT, ADANSONIA DIGITATA SEED OIL, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, WATER, BUTYLENE GLYCOL, ALOE BARBADENSIS LEAF EXTRACT

  • 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.

  • Keep out of reach of children.

    If product is swallowed, get medical help or contact a Poison Control Center right away.

  • Purpose

    Sunscreen

  • SunPrise Mild Airy Finish Sunstick_Outer Package Box

    SunPrise Mild Airy Finish Sunstick_Outer Package Box

  • INGREDIENTS AND APPEARANCE
    ETUDE SUNPRISE MILD AIRY FINISH SUNSTICK 
    avobenzone, homosalate, octisalate, octocrylene stick
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84468-743
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE4.5 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE5 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE9.5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    DIETHYLHEXYL CARBONATE (UNII: YCD50O0Z6L)  
    ISOPROPYL PALMITATE (UNII: 8CRQ2TH63M)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84468-743-021 in 1 BOX03/15/2025
    119 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02003/15/2025
    Labeler - ETUDE CORPORATION (687847335)
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