Label: NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BODY SPF 60 PLUS- avobenzone, homosalate, octisalate, octocrylene aerosol, spray

  • NDC Code(s): 69968-0778-5
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated October 20, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Avobenzone 3%Sunscreen
    Homosalate 10%Sunscreen
    Octisalate 5%Sunscreen
    Octocrylene 10%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.
    • Keep away from face to avoid breathing it

    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

    Warning

    FLAMMABLE. Contents under pressure. Do not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperature below 120°F (48°C). Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

  • Directions

    • shake well before and frequently during use
    • spray liberally and spread evenly by hand 15 minutes before sun exposure
    • hold container 4-6 inches from the skin to apply. Rub in.
    • do not spray directly into face. Spray on hands and then apply to face. Rub in.
    • do not apply in windy conditions.
    • use in well-ventilated area
    • 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

    Alcohol Denat., Isobutane, Dicaprylyl Carbonate, Zingiber Officinale (Ginger) Root Extract, Tocopheryl Acetate, Polyester-7, Acrylates/Octylacrylamide Copolymer, Neopentyl Glycol Diheptanoate, Fragrance

  • Questions?

    Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com

  • SPL UNCLASSIFIED SECTION

    Distributed by:

    JOHNSON & JOHNSON CONSUMER INC.

    Skillman, NJ 08558

  • PRINCIPAL DISPLAY PANEL - 141 g Can Label

    Neutrogena®

    DERMATOLOGIST RECOMMENDED BRAND

    Invisible Daily

    defence

    body spray

    sunscreen

    BROAD SPECTRUM SPF 60+

    60+

    sun + environment

    oxybenzone free

    water resistant (80 minutes)

    NET WT. 5.0 OZ (141 g)

    Neutrogena_01

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BODY SPF 60 PLUS 
    avobenzone, homosalate, octisalate, octocrylene aerosol, spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0778
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
    HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    ALCOHOL (UNII: 3K9958V90M)  
    ISOBUTANE (UNII: BXR49TP611)  
    GINGER (UNII: C5529G5JPQ)  
    POLYESTER-7 (UNII: 0841698D2F)  
    ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0778-5141 g in 1 CAN; Type 0: Not a Combination Product12/05/2022
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/05/2022
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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