Label: COPPERTONE EVERY TONE BRIGHTENING SUNSCREEN SPF 60- avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% lotion

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

Drug Label Information

Updated December 31, 2025

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  • Drug Facts

  • Active ingredients

    Avobenzone 3%, Homosalate 15%,
    Octisalate 5%, Octocrylene 10%

  • Purpose

    Sunscreen

  • Uses

    ■ helps prevent sunburn

  • Warnings

    For external use only

  • DO NOT USE

    Do not use ondamaged or broken skin

  • WHEN USING

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

  • STOP USE

    Stop use and ask a doctor ifrash 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 at least every 2 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-sleeve shirts, pants, hats, and sunglasses
    ■ 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

    dicaprylyl carbonate, butylene glycoldicaprylate/dicaprate, silica dimethyl silylate, neopentyl glycoldiheptanoate, dibutyl adipate, dimethicone, dextrin palmitate, coco-caprylate/caprate, acetyl ethylhexyl polyhydroxystearate, butyloctylsalicylate, diethylhexyl 2,6-naphthalate, diisopropyl adipate, poly C10-30alkyl acrylate, triheptanoin, silica, alcohol denat., 4-butylresorcinol,dimethicone/vinyl dimethicone crosspolymer, niacinamide, stearalkoniumhectorite, dimethicone crosspolymer, C12-15 alkyl benzoate, 12-hydroxy
    stearic acid, dilinoleic acid/butanediol copolymer, propylene carbonate,ethylhexyl palmitate, hydroxyacetophenone, quaternium-90 bentonite,fragrance, stearic acid, castor oil/IPDI copolymer, water, palmitic acid

  • Questions?

    1-866-288-3330

  • PRINCIPAL DISPLAY PANEL

    NEW

    Coppertone ®Clear Sunscreen

    Every Tone Invisible Finish

    Face 60+

    Brightening UV Defense plus Niacinamide

    Transparent on all skin tones

    Won't clog pores

    Broad Specturn SPF 60+

    1.7 FL OZ (50 mL)

    CTN Brightening 60+ Lotion

  • INGREDIENTS AND APPEARANCE
    COPPERTONE EVERY TONE BRIGHTENING SUNSCREEN SPF 60 
    avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66800-8000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (HARD PARTICLE) (UNII: H895X08VNQ)  
    DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    QUATERNIUM-90 BENTONITE (UNII: 97K5YEF88C)  
    STEARALKONIUM HECTORITE (UNII: OLX698AH5P)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    FRAGRANCE FRESH CITRUS FLORAL ORC1501495 (UNII: OU4GI2R2WB)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    POLYVINYL ALCOHOL/POLYVINYL ACETATE COPOLYMER (8:1; 50000 MW) (UNII: 8K8B5SD7ZR)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    CALCIUM SILICATE (UNII: S4255P4G5M)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)  
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    ALCOHOL (UNII: 3K9958V90M)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
    CASTOR OIL/IPDI COPOLYMER (UNII: GSA2TXZ34G)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    TRIHEPTANOIN (UNII: 2P6O7CFW5K)  
    C12-20 ALKYL BENZOATE (UNII: Y15I6XI14C)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    DIBUTYL ADIPATE (UNII: F4K100DXP3)  
    4-BUTYLRESORCINOL (UNII: 2IK4UQ3ZGA)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66800-8000-11 in 1 CARTON10/15/2024
    150 g in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/15/2024
    Labeler - Beiersdorf Inc (001177906)
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