NEUTROGENA HYDROBOOST WATER GEL SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion 
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 ® Hydro Boost water gel lotion BROAD SPECTRUM SPF 50

Drug Facts

Active IngredientsPurpose
Avobenzone (2.7%)Sunscreen
Homosalate (9%)Sunscreen
Octisalate (5%)Sunscreen
Octocrylene (9%)Sunscreen
Oxybenzone (4.5%)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 15 minutes before sun exposure
  • 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 value of SPF 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, Alcohol Denat., Caprylyl Methicone, Diisopropyl Adipate, Silica, Dicaprylyl Carbonate, Dimethicone, Polyurethane-62, Phenoxyethanol, Hydroxyacetophenone, Pentylene Glycol, Aluminum Starch Octenylsuccinate, Sodium Acryloyldimethyltaurate/VP Crosspolymer, Acrylates/Dimethicone Copolymer, Glyceryl Stearate, Fragrance, Chlorphenesin, Menthyl Lactate, Tocopheryl Acetate, Disodium EDTA, Trideceth-6, Hydrolyzed Hyaluronic Acid, Sodium Hydroxide, Violet 2,Blue 1

Questions or comments?

Call toll-free 800-299-4786 or 215-273-875 (collect) www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena ®

#1 DERMATOLOGIST RECOMMENDED BRAND

Hydro
Boost
water gel lotion

sunscreen

BROAD SPECTRUM SPF 50

50

helioplex ®

broad spectrum uva.uvb

invisible finish
non-greasy

water resistant(80 minutes)

3.0 fl. oz. (88 mL)

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label
NEUTROGENA HYDROBOOST WATER GEL SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0315
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE27 mg  in 1 mL
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE90 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE90 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE45 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
ALCOHOL (UNII: 3K9958V90M)  
GLYCERIN (UNII: PDC6A3C0OX)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
HYDROXYACETOPHENONE (UNII: G1L3HT4CMH)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
D&C VIOLET NO. 2 (UNII: 350KA7O6HK)  
FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0315-388 mL in 1 TUBE; Type 0: Not a Combination Product10/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/01/2017
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 9/2022
Document Id: e7edeb0c-eba2-a690-e053-2995a90ae271
Set id: 986126cb-f4e7-4cff-ba5d-a2e4e4c72847
Version: 6
Effective Time: 20220905
 
Johnson & Johnson Consumer Inc.