Label: NEUTROGENA BEACH DEFENSE WATER PLUS SUN PROTECTION SUNSCREEN BROAD SPECTRUM SPF30- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone spray

  • NDC Code(s): 69968-0101-6, 69968-0101-8
  • Packager: Kenvue Brands LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 11, 2024

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active ingredients

    Avobenzone 3%
    Homosalate 8%
    Octisalate 4%
    Octocrylene 2%
    Oxybenzone 5%

  • Purpose

    Sunscreen

  • Uses

    • helps prevent sunburn Sunscreen
    • 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 away from face to avoid breathing it
      • 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.

    • Caution: 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

    • spray liberally and spread evenly by hand 15 minutes before sun exposure
    • apply to all skin exposed to the sun
    • 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 a 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, dimethicone, acrylates/octylacrylamide copolymer, trisiloxane, diethylhexyl 2,6 naphthalate, tocopheryl acetate, fragrance

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 240 g Can Label

    FAMILY SIZE
    20% MORE

    Neutrogena ®

    Beach
    Defense ®

    water + sun
    protection

    SUNSCREEN SPRAY

    Broad Spectrum SPF30

    30

    helioplex ®
    broad spectrum uva-uvb

    water resistant
    (80 minutes)

    #1 DERMATOLOGIST
    RECOMMENDED SUNCARE

    NET WT. 8.5 OZ. (240g)

    PRINCIPAL DISPLAY PANEL - 240 g Can Label
  • INGREDIENTS AND APPEARANCE
    NEUTROGENA BEACH DEFENSE WATER PLUS SUN PROTECTION  SUNSCREEN BROAD SPECTRUM SPF30
    avobenzone, homosalate, octisalate, octocrylene, and oxybenzone spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0101
    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) HOMOSALATE30 mg  in 1 g
    OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE40 mg  in 1 g
    OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE20 mg  in 1 g
    OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE50 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
    ALCOHOL (UNII: 3K9958V90M)  
    ISOBUTANE (UNII: BXR49TP611)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0101-8240 g in 1 CAN; Type 0: Not a Combination Product10/01/2016
    2NDC:69968-0101-6184 g in 1 CAN; Type 0: Not a Combination Product10/01/2016
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/01/2016
    Labeler - Kenvue Brands LLC (118772437)