NEUTROGENA HYDRO BOOST WATER SUNSCREEN BROAD SPECTRUM SPF 15- avobenzone, homosalate, octisalate, and octocrylene gel 
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.

----------

Neutrogena ® Hydro Boost water gel with sunscreen BROAD SPECTRUM SPF 15

Drug Facts

Active ingredientsPurpose
Avobenzone 2%Sunscreen
Homosalate 4%Sunscreen
Octisalate 4%Sunscreen
Octocrylene 2%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

For sunscreen use:

  • apply generously and evenly 15 minutes before sun exposure
  • reapply at least every 2 hours
  • use a water resistant sunscreen if swimming or sweating
  • 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

Water, Glycerin, Caprylyl Methicone, Methyl Methacrylate Crosspolymer, Pentylene Glycol, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Benzyl Alcohol, Glyceryl Stearate, Chlorphenesin, Sodium Hyaluronate, Disodium EDTA, Fragrance, Sodium Hydroxide, Blue 1, Red 40

Questions?

Call toll-free 800-582-4048 or 215-273-8755 (collect) or visit www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

Hydro Boost
water gel
with
sunscreen
BROAD SPECTRUM
SPF 15

boosts hydration for smooth, supple skin

Neutrogena ®
DERMATOLOGIST RECOMMENDED

1.7 FL OZ (50mL)

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton
NEUTROGENA HYDRO BOOST WATER SUNSCREEN BROAD SPECTRUM SPF 15 
avobenzone, homosalate, octisalate, and octocrylene gel
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0029
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE20 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE40 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE40 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE20 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
GLYCERIN (UNII: PDC6A3C0OX)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
METHYL METHACRYLATE/GLYCOL DIMETHACRYLATE CROSSPOLYMER (UNII: EG97988M5Q)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0029-11 in 1 CARTON10/01/201512/23/2021
150 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/01/201512/23/2021
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 3/2022
Document Id: da53c4fb-d410-2fe7-e053-2a95a90adfa7
Set id: 4f8bd3d1-15d0-4ed5-baa7-bc253adcae97
Version: 7
Effective Time: 20220316
 
Johnson & Johnson Consumer Inc.