NEUTROGENA BEACH DEFENSE WATER PLUS SUN PROTECTION SUNSCREEN BROAD SPECTRUM SPF50 PLUS- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone stick 
Johnson & Johnson Consumer Inc.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Neutrogena® Beach Defense® water+ sun protection SUNSCREEN STICK Broad Spectrum SPF 50+

Drug Facts

Active ingredientPurpose
Avobenzone 3%Sunscreen
Homosalate 15%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 10%Sunscreen
Oxybenzone 3%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

Inactive ingredients

Octyldodecyl Neopentanoate, Neopentyl Glycol Diethylhexanoate, Polyethylene, Beeswax, Ozokerite, Paraffin, C12-15 Alkyl Benzoate, Adipic Acid/Diglycol Crosspolymer, Neopentyl Glycol Diisostearate, Dimethicone, Fragrance, Diethylhexyl 2,6-Naphthalate, BHT

Questions?

800-299-4786; Outside US, dial collect 215-273-8755 or www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 42 g Canister Label

Neutrogena®

Beach
Defense®
water + sun protection

SUNSCREEN STICK
Broad Spectrum SPF50 +

50+

helioplex®
broad spectrum uva•uvb

NET WT. 1.5 OZ. (42g)

PRINCIPAL DISPLAY PANEL - 42 g Canister Label
NEUTROGENA BEACH DEFENSE WATER PLUS SUN PROTECTION SUNSCREEN BROAD SPECTRUM SPF50 PLUS 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone stick
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0418
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
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone30 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
Octyldodecyl Neopentanoate (UNII: X8725R883T)  
Neopentyl Glycol Diethylhexanoate (UNII: U68ZV6W62C)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
Paraffin (UNII: I9O0E3H2ZE)  
ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
ADIPIC ACID/DIGLYCOL CROSSPOLYMER (20000 MPA.S) (UNII: R9TPS68K19)  
Neopentyl Glycol Diisostearate (UNII: 4M6OQ34JWW)  
Dimethicone (UNII: 92RU3N3Y1O)  
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0418-142 g in 1 CANISTER; Type 0: Not a Combination Product10/01/201311/24/2021
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35210/01/201311/24/2021
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 7/2020
Document Id: 464080ae-98a4-4ed1-a20b-5595c9baa6ab
Set id: b5d5a33f-ca85-42fe-a7a7-a13adb229366
Version: 2
Effective Time: 20200723
 
Johnson & Johnson Consumer Inc.