NEUTROGENA WET SKIN KIDS SUNSCREEN BROAD SPECTRUM SPF70 PLUS- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone aerosol, spray 
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® Wet Skin kids BEACH & POOL sunscreen spray BROAD SPECTRUM SPF 70+

Drug Facts

Active ingredientsPurpose
Avobenzone 3%Sunscreen
Homosalate 15%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 10%Sunscreen
Oxybenzone 6%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 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

  • shake well before and frequently during use
  • 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., Dimethyl Ether, Octyldodecyl Citrate Crosspolymer, Ethyl Methicone, Acrylates/Octylacrylamide Copolymer, Dimethicone, Acrylates/Dimethicone Copolymer, Fragrance, Tocopheryl Acetate, Diethylhexyl 2,6-Naphthalate, Nelumbo Nucifera Flower Wax, Cetyl Dimethicone/Bis-Vinyldimethicone Crosspolymer, Ascorbyl Palmitate

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 141 g Can Label

Neutrogena ®
#1 DERMATOLOGIST RECOMMENDED BRAND
Wet Skin
kids
BEACH & POOL
sunscreen spray
BROAD SPECTRUM SPF 70+

70+

helioplex ®
broad spectrum uva•uvb

full strength protection
on wet or dry skin
hypoallergenic
water-resistant (80 minutes)

NET WT 5.0 OZ (141 g)

PRINCIPAL DISPLAY PANEL - 141 g Can Label
NEUTROGENA WET SKIN KIDS  SUNSCREEN BROAD SPECTRUM SPF70 PLUS
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0091
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) OXYBENZONE60 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ASCORBYL PALMITATE (UNII: QN83US2B0N)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
DIMETHYL ETHER (UNII: AM13FS69BX)  
ETHYL METHICONE (8 MPA.S) (UNII: 3YWG8XYT8H)  
NELUMBO NUCIFERA FLOWER WAX (UNII: U01S6C427I)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0091-1141 g in 1 CAN; Type 0: Not a Combination Product11/01/201503/27/2023
2NDC:69968-0091-22 in 1 CARTON11/01/201507/29/2023
2141 g in 1 CAN; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35211/01/201507/29/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 3/2023
Document Id: f5e63dcd-1835-d0b7-e053-2995a90a7259
Set id: a775e6ad-6067-46f6-b172-4152ae48b503
Version: 6
Effective Time: 20230302
 
Johnson & Johnson Consumer Inc.