Label: NEUTROGENA CLEAR BODY BREAKOUT FREE OIL FREE SUNSCREEN BROAD SPECTRUM SPF 30- avobenzone, homosalate, octisalate, and octocrylene lotion

  • NDC Code(s): 69968-0572-5
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 17, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Avobenzone 2.5%Sunscreen
    Homosalate 8%Sunscreen
    Octisalate 5%Sunscreen
    Octocrylene 8%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 reach of children. If swallowed, get medical help or contact a Poison Control Center right away
  • Directions

    • apply generously and evenly 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 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-sleeved shirts, pants, hats, and sunglasses
    • Children under 6 months of age: Ask a doctor
  • Other information

    • protect this product from excessive heat and direct sun
    • may stain some fabrics
  • Inactive ingredients

    Water, Silica, Cetyl Dimethicone, Styrene/Acrylates Copolymer, C12-15 Alkyl Benzoate, Ethylhexylglycerin, Steareth-100, Aluminum Starch Octenylsuccinate, Phenoxyethanol, Caprylyl, Glycol, Sodium Polyacrylate, Dimethicone, Polyester-7, Chlorphenesin, Steareth-2, Ethylhexyl Stearate, Disodium EDTA, Propylene Glycol, Neopentyl Glycol Diheptanoate, Bisabolol, Acrylates/Dimethicone Copolymer, Butylene Glycol, BHT, Mannan, Xanthan Gum, Capryloyl, Glycine, Trideceth-6, Sarcosine, Cedrus Atlantica Bark Extract, Cinnamomum Zeylanicum Bark Extract, Portulaca Oleracea Extract

  • Questions?

    Visit www.neutrogena.com or call toll‐free 800-299-4786 or 215‐273‐8755 (collect)

  • SPL UNCLASSIFIED SECTION

    Distributed by: JOHNSON & JOHNSON CONSUMER INC. Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 147 mL Tube Label

    Neutrogena ®

    DERMATOLOGIST RECOMMENDED BRAND

    Clear Body

    BREAKOUT FREE

    oil-free

    sunscreen

    BROAD SPECTRUM SPF 30

    30

    helioplex ®

    broad spectrum uva•uvb

    won't cause breakouts

    oxybenzone free

    water resistant (80 minutes)

    5.0 FL OZ (147 mL)

    Neutrogena_01

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA CLEAR BODY BREAKOUT FREE OIL FREE SUNSCREEN BROAD SPECTRUM SPF 30 
    avobenzone, homosalate, octisalate, and octocrylene lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0572
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE25 mg  in 1 mL
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE80 mg  in 1 mL
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE80 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    STEARETH-100 (UNII: 4OH5W9UM87)  
    ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    POLYESTER-7 (UNII: 0841698D2F)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    STEARETH-2 (UNII: V56DFE46J5)  
    ETHYLHEXYL STEARATE (UNII: EG3PA2K3K5)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    YEAST MANNAN (UNII: 91R887N59P)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CAPRYLOYL GLYCINE (UNII: 8TY5YO42NJ)  
    TRIDECETH-6 (UNII: 3T5PCR2H0C)  
    SARCOSINE (UNII: Z711V88R5F)  
    CEDRUS ATLANTICA BARK (UNII: ITP1Q41UPF)  
    CINNAMON BARK OIL (UNII: XE54U569EC)  
    PURSLANE (UNII: M6S840WXG5)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0572-5147 mL in 1 TUBE; Type 0: Not a Combination Product10/07/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/07/2019
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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