Label: NEUTROGENA BEACH DEFENSE WATER PLUS SUN PROTECTION SUNSCREEN STICK BROAD SPECTRUM SPF 50 PLUS- avobenzone, homosalate, octisalate, and octocrylene spray

  • NDC Code(s): 69968-0574-2, 69968-0574-3
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 21, 2023

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

View All Sections
  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Avobenzone 3%Sunscreen
    Homosalate 15%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.

    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 liberally and evenly 15 minutes before sun exposure
    • ensure complete coverage to the area above the lip, nose and tops of ears
    • 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
    • After use, twist stick down prior to capping to ensure complete closure.
  • Other information

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

    Neopentyl Glycol Diethylhexanoate, Octyldodecyl Neopentanoate, Polyethylene, Isohexadecane, Butyloctyl Salicylate, Ozokerite, Paraffin, Synthetic Beeswax, C12-15 Alkyl Benzoate, VP/Eicosene Copolymer, Neopentyl Glycol Diisostearate, Dimethicone, Diethylhexyl 2,6-Naphthalate, Styrene/Acrylates Copolymer, Fragrance, BHT

  • 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 - 42 g Canister Label

    Neutrogena ®

    DERMATOLOGIST RECOMMENDED BRAND

    Beach

    Defense ®

    water + sun protection

    sunscreen stick

    BROAD SPECTRUM SPF 50+

    50+

    helioplex ®

    broad spectrum uva•uvb

    water resistant (80minutes)

    NET WT. 1.5 OZ. (42 g)

    Ntg_001

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA BEACH DEFENSE WATER PLUS SUN PROTECTION SUNSCREEN STICK BROAD SPECTRUM SPF 50 PLUS 
    avobenzone, homosalate, octisalate, and octocrylene spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0574
    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) HOMOSALATE150 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
    NEOPENTYL GLYCOL DIETHYLHEXANOATE (UNII: U68ZV6W62C)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    CERESIN (UNII: Q1LS2UJO3A)  
    PARAFFIN (UNII: I9O0E3H2ZE)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    NEOPENTYL GLYCOL DIISOSTEARATE (UNII: 4M6OQ34JWW)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    YELLOW WAX (UNII: 2ZA36H0S2V)  
    EICOSYL POVIDONE (UNII: XQQ9MKE2BJ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0574-242 g in 1 CANISTER; Type 0: Not a Combination Product10/07/2019
    2NDC:69968-0574-32 in 1 CARTON10/07/2019
    242 g in 1 CANISTER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/07/2019
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!