NEUTROGENA ULTRA SHEER FACE MIST SUNSCREEN BROAD SPECTRUM SPF 55- avobenzone, homosalate, octisalate, and octocrylene 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 ® Ultra Sheer ® face mist sunscreen BROAD SPECTRUM SPF 55

Drug Facts

Active ingredientsPurpose
Avobenzone 3%Sunscreen
Homosalate 10%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 10%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

  • Danger: Flammable. Do not use near fire, heat or while smoking. Do not incinerate. Store at temperature below 120°F (48°C).

Directions

  • spray liberally and spread evenly by hand 15 minutes before sun exposure
  • 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., Dimethicone, Trisiloxane, Diisopropyl Adipate, Acrylates/Octylacrylamide Copolymer, Acrylates/Dimethicone Copolymer, Fragrance, Tocopheryl Acetate

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 - 100 mL Bottle Label

New
Neutrogena ®
#1 DERMATOLOGIST RECOMMENDED BRAND
Ultra Sheer ®
Face
mist
sunscreen
BROAD SPECTRUM SPF 55

55
helioplex ®
broad spectrum uva•uvb
instantly refreshes + protects
invisible finish, oil-free
water resistant (40minutes)

3.4 FL OZ (100 mL)

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label
NEUTROGENA ULTRA SHEER FACE MIST SUNSCREEN BROAD SPECTRUM SPF 55 
avobenzone, homosalate, octisalate, and octocrylene spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0543
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) HOMOSALATE100 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0543-3100 mL in 1 BOTTLE; Type 0: Not a Combination Product10/07/2019
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/07/2019
Labeler - Johnson & Johnson Consumer Inc. (002347102)

Revised: 12/2021
Document Id: d3924f6a-cafd-8858-e053-2a95a90a0df4
Set id: 53420c81-251b-4038-a7a9-29c263369870
Version: 3
Effective Time: 20211220
 
Johnson & Johnson Consumer Inc.