NEUTROGENA ULTRA SHEER DRY TOUCH SUNSCREEN BROAD SPECTRUM SPF70- 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 ® Ultra Sheer ® dry-touch sunscreen BROAD SPECTRUM SPF 70

Drug Facts

Active ingredientsPurpose
Avobenzone 3%Sunscreen
Homosalate 15%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 2.8%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 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 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
  • protect from freezing

Inactive ingredients

Water, Styrene/Acrylates Copolymer, Silica, Diethylhexyl 2,6-Naphthalate, Beeswax, Caprylyl Methicone, Cetyl Dimethicone, Ethylhexylglycerin, Glyceryl Stearate, PEG-100 Stearate, Sodium Polyacrylate, Acrylates/C12-22 Alkyl Methacrylate Copolymer, Dimethicone, Xanthan Gum, Trimethylsiloxysilicate, Disodium EDTA, Fragrance, Dipotassium Glycyrrhizate, BHT, Methylisothiazolinone, Polyaminopropyl Biguanide

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 - 88 mL Tube Label

Neutrogena ®
#1 DERMATOLOGIST RECOMMENDED BRAND
Ultra Sheer ®
dry-touch
sunscreen

BROAD SPECTRUM SPF 70
70

helioplex ®
broad spectrum uva•uvb

lightweight clean feel
fast drying
water resistant (80 minutes)

3.0 FL OZ (88mL)

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label
NEUTROGENA ULTRA SHEER DRY TOUCH  SUNSCREEN BROAD SPECTRUM SPF70
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0168
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) HOMOSALATE150 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE28 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
YELLOW WAX (UNII: 2ZA36H0S2V)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
PEG-100 STEARATE (UNII: YD01N1999R)  
POLIHEXANIDE (UNII: 322U039GMF)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
WATER (UNII: 059QF0KO0R)  
XANTHAN GUM (UNII: TTV12P4NEE)  
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0168-388 mL in 1 TUBE; Type 0: Not a Combination Product01/01/200706/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/01/200706/15/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: f308b818-2c28-1140-e053-2995a90adb4b
Set id: 837e1f94-5335-48dd-9424-71996c366b39
Version: 6
Effective Time: 20230124
 
Johnson & Johnson Consumer Inc.