NEUTROGENA OIL-FREE MOISTURE  SUNSCREEN BROAD SPECTRUM SPF 35- 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® oil-free moisture sunscreen BROAD SPECTRUM SPF 35

Drug Facts

Active ingredients

Avobenzone 3%
Homosalate 12%
Octisalate 5%
Octocrylene 2.35%
Oxybenzone 6%

Purpose

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

  • Pump onto fingers and apply over face and neck daily after cleansing. Works well alone, under makeup, or over a serum.
  • For Sunscreen Use:
    • apply liberally 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, Dimethicone, Diethylhexyl 2,6-Naphthalate, Glycerin, Trisiloxane, Potassium Cetyl Phosphate, Glyceryl Stearate, PEG-100 Stearate, Cetearyl Alcohol, Caprylyl Methicone, Behenyl Alcohol, Styrene/Acrylates Copolymer, Benzyl Alcohol, Ethylhexylglycerin, Methylparaben, Cetearyl Glucoside, Xanthan Gum, Propylparaben, Disodium EDTA, BHT, Methylisothiazolinone

Questions or comments?

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

Dist. by Neutrogena Corp.
Los Angeles, CA 90045

PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton

oil-free
moisture

with
sunscreen

BROAD SPECTRUM
SPF 35

facial moisturizer
with UVA/UVB protection

non-comedogenic
(won't clog pores)
Neutrogena®

DERMATOLOGIST RECOMMENDED

2.5 FL. OZ. (73mL)

PRINCIPAL DISPLAY PANEL - 73 mL Bottle Carton
NEUTROGENA OIL-FREE MOISTURE  SUNSCREEN BROAD SPECTRUM SPF 35
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:10812-106
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Avobenzone (UNII: G63QQF2NOX) (Avobenzone - UNII:G63QQF2NOX) Avobenzone30 mg  in 1 mL
Homosalate (UNII: V06SV4M95S) (Homosalate - UNII:V06SV4M95S) Homosalate120 mg  in 1 mL
Octisalate (UNII: 4X49Y0596W) (Octisalate - UNII:4X49Y0596W) Octisalate50 mg  in 1 mL
Octocrylene (UNII: 5A68WGF6WM) (Octocrylene - UNII:5A68WGF6WM) Octocrylene23.5 mg  in 1 mL
Oxybenzone (UNII: 95OOS7VE0Y) (Oxybenzone - UNII:95OOS7VE0Y) Oxybenzone60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
Water (UNII: 059QF0KO0R)  
Dimethicone (UNII: 92RU3N3Y1O)  
Trisiloxane (UNII: 9G1ZW13R0G)  
Diethylhexyl 2,6-Naphthalate (UNII: I0DQJ7YGXM)  
Glycerin (UNII: PDC6A3C0OX)  
Potassium Cetyl Phosphate (UNII: 03KCY6P7UT)  
Glyceryl Monostearate (UNII: 230OU9XXE4)  
PEG-100 Stearate (UNII: YD01N1999R)  
Cetostearyl Alcohol (UNII: 2DMT128M1S)  
Docosanol (UNII: 9G1OE216XY)  
Ethylhexylglycerin (UNII: 147D247K3P)  
Benzyl Alcohol (UNII: LKG8494WBH)  
Caprylyl Trisiloxane (UNII: Q95M2P1KJL)  
Methylparaben (UNII: A2I8C7HI9T)  
Cetearyl Glucoside (UNII: 09FUA47KNA)  
Xanthan Gum (UNII: TTV12P4NEE)  
Propylparaben (UNII: Z8IX2SC1OH)  
Edetate Disodium (UNII: 7FLD91C86K)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
Methylisothiazolinone (UNII: 229D0E1QFA)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:10812-106-021 in 1 CARTON06/01/201010/02/2018
173 mL in 1 BOTTLE, PUMP; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH NOT FINALpart35206/01/201010/02/2018
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 11/2017
 
Johnson & Johnson Consumer Inc.