Label: COPPERTONE TANNING SUNSCREEN SPF 8- avobenzone 2%, homosalate 5%, octisalate 4.5%, octocrylene 3% lotion

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

Drug Label Information

Updated January 16, 2024

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  • Drug Facts

  • Active ingredients

    Avobenzone 2%, Homosalate 5%, Octisalate 4.5%, Octocrylene 3%

  • Purpose

    Sunscreen

  • Use

    ■ helps prevent sunburn

  • Warnings

    Skin Cancer/Skin Aging Alert: Spending time in the sun increases your risk of skin cancer and early skin aging. This product has been shown only to help prevent sunburn, not skin cancer or early skin aging.

    For external use only

  • DO NOT USE

    Do not use on damaged or broken skin

  • WHEN USING

    When using this product keep out of eyes. Rinse with water to remove.

  • STOP USE

    Stop use and ask a doctor if rash occurs

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • 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

    ■ children under 6 months: Ask a doctor

  • Other information

    ■ protect this product from excessive heat and direct sun

    ■ may stain or damage some fabrics or surfaces

  • Inactive ingredients

    water, aluminum starch octenylsuccinate, glycerin, silica, phenoxyethanol, isododecane, polyester-27, styrene/acrylates copolymer, ethylhexylglycerin, acrylates/C10-30 alkyl acrylate crosspolymer, arachidyl alcohol, neopentyl glycol diheptanoate, glyceryl stearate, PEG-100 stearate, beeswax, fragrance, behenyl alcohol, arachidyl glucoside, potassium hydroxide, disodium EDTA

  • Questions?

    1-866-288-3330

  • PRINCIPAL DISPLAY PANEL

    Coppertone Sunscreen Lotion

    Tanning 8

    Moisturizes Skin for a Radiant Tan

    Lightweight, non-greasy

    Free of Oxybenzone, Octinoxate, Dyes & PABA

    Water Resistant (80 Minutes)

    Broad Spectrum SPF 8

    Tanning 8

  • INGREDIENTS AND APPEARANCE
    COPPERTONE TANNING SUNSCREEN SPF 8 
    avobenzone 2%, homosalate 5%, octisalate 4.5%, octocrylene 3% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66800-7034
    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) OCTOCRYLENE3 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE2 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    STYRENE/ACRYLAMIDE COPOLYMER (500000 MW) (UNII: 5Z4DPO246A)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    GLYCERYL STEARATE SE (UNII: FCZ5MH785I)  
    ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    FRAGRANCE FLORAL ORC0902236 (UNII: R66Z4YW3X0)  
    DISODIUM EDTA-COPPER (UNII: 6V475AX06U)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    POLYESTER-7 (UNII: 0841698D2F)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    SYNTHETIC BEESWAX (UNII: 08MNR5YE2R)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    POTASSIUM HYDROXIDE (UNII: WZH3C48M4T)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ISODODECANE (UNII: A8289P68Y2)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66800-7034-8237 g in 1 BOTTLE, PLASTIC; Type 0: Not a Combination Product01/31/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/31/2024
    Labeler - Beiersdorf Inc (001177906)
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