Label: COPPERTONE EVERYTONE FACE SUNSCREEN SPF 55- avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% lotion

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

Drug Label Information

Updated December 30, 2023

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

  • Drugs Facts

  • Active ingredients

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

  • Purpose

    Sunscreen

  • Use

    ■ helps prevent sunburn

  • Warnings

    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 40 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 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 glycol dicaprylate/dicaprate, neopentyl glycol diheptanoate, silica dimethyl silylate, dibutyl adipate, dimethicone, dextrin palmitate, coco-caprylate/caprate, acetyl ethylhexyl polyhydroxystearate, butyloctyl salicylate, diethylhexyl 2,6-naphthalate, diisopropyl adipate, poly C10-30 alkyl acrylate, triheptanoin, silica, alcohol denat., dimethicone/vinyl dimethicone crosspolymer, stearalkonium hectorite, 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

    Coppertone ® Clear Sunscreen

    EveryTone

    Invisible Finish Face

    55

    Transparent on Skin

    For All Skin Tones

    Won't Clog Pores

    Water Resistant (40 Minutes)

    Broad Spectrum SPF 55

    EveryTone Face

  • INGREDIENTS AND APPEARANCE
    COPPERTONE EVERYTONE FACE SUNSCREEN SPF 55 
    avobenzone 3%, homosalate 15%, octisalate 5%, octocrylene 10% lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66800-1094
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE15 g  in 100 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE10 g  in 100 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE5 g  in 100 g
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE3 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    PROPYLENE CARBONATE (UNII: 8D08K3S51E)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
    ACRYLATES/C10-30 ALKYL ACRYLATE CROSSPOLYMER (60000 MPA.S) (UNII: 8Z5ZAL5H3V)  
    TRIHEPTANOIN (UNII: 2P6O7CFW5K)  
    COCO-CAPRYLATE/CAPRATE (UNII: 8D9H4QU99H)  
    HYDROGENATED CASTOR OIL (UNII: ZF94AP8MEY)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    12-HYDROXYSTEARIC ACID (UNII: 933ANU3H2S)  
    ETHYLHEXYL PALMITATE (UNII: 2865993309)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    ISOPHORONE DIISOCYANATE (UNII: 43B0856528)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    DILINOLEIC ACID/BUTANEDIOL COPOLYMER (UNII: 1F2S8T535O)  
    WATER (UNII: 059QF0KO0R)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
    FRAGRANCE CLEAN ORC0600327 (UNII: 329LCV5BTF)  
    ALCOHOL (UNII: 3K9958V90M)  
    BUTYLENE GLYCOL DICAPRYLATE/DICAPRATE (UNII: 75D21FL1PI)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    QUATERNIUM-90 BENTONITE (UNII: 97K5YEF88C)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    SILICA DIMETHYL SILYLATE (UNII: EU2PSP0G0W)  
    DIBUTYL ADIPATE (UNII: F4K100DXP3)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    Product Characteristics
    Colorwhite (white to off-white) Score    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66800-1094-259 g in 1 TUBE; Type 0: Not a Combination Product11/01/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02011/01/2023
    Labeler - Beiersdorf Inc (001177906)