ULTA SUN DRY TOUCH SPF 70 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [ULTA]

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  • ULTA SUN DRY TOUCH SPF 70 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [ULTA]

ULTA SUN DRY TOUCH SPF 70 (AVOBENZONE, HOMOSALATE, OCTISALATE, OCTOCRYLENE, OXYBENZONE) LOTION [ULTA]
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NDC 62296-8900-4
Set ID 4a89873c-7339-428d-8b67-7b96ef5c5b1b
Category HUMAN OTC DRUG LABEL
Packager Ulta
Generic Name
Product Class
Product Number
Application Number PART352
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  • ACTIVE INGREDIENT

    AVOBENZONE 3.0%, HOMOSALATE 15.0%, OCTISALATE 5.0%, OCTOCRYLENE 2.8%,

    OXYBENZONE 6.0%

  • 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 the reach of children

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

    • May stain some fabrics
  • Directions

    • apply liberally 15 minutes before sun exposure
    • reapply: after 80 minutes of swimming or sweating
    • immediately after towel drying
    • at least every 2 hours
    • 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 of 15 or higher and other sun protection measures including:
    • limit time in the sun, especially from 10:00 a.m. - 2 p.m.
    • wear long-sleeve shirts, pants, hats and sunglasses
    • children under 6 months of age: Ask a doctor
  • Inactive ingredients

    Water, Styrene/Acrylates Copolymer, Butyloctyl Salicylate, Silica, Glyceryl Stearate, PEG-100 Stearate, Caprylyl Methicone, Sodium Polyacrylate, Benzyl Alcohol, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Ethylhexyl Stearate, Beeswax, Dimethicone, Chlorphenesin, Cetyl Dimethicone, Xanthan Gum, Trimethylsiloxysilicate, Fragrance, Trideceth-6, Disodium EDTA, BHT, Dipotassium Glycyrrhizate.

  • Other information

    • protect this product from excessive heat and direct sun
  • Principal Display Panel


    62296-8900-4

    SUNCARE

    BROAD SPECTRUM

    SPF 70

    WATER RESISTANT

    (80 MINUTES)

    LIGHT WEIGHT

    SUNSCREEN LOTION

    SHEER

    ULTA

    5 fl oz/147 ml


    Label






  • INGREDIENTS AND APPEARANCE
    ULTA SUN DRY TOUCH SPF 70 
    avobenzone, homosalate, octisalate, octocrylene, oxybenzone lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62296-8900
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE2.8 g  in 100 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE6 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    BENZYL ALCOHOL (UNII: LKG8494WBH)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62296-8900-4147 g in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35201/25/2016
    Labeler - Ulta (608168597)
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