Neutrogena ® Invisible Daily defense face mist Sunscreen Broad Spectrum SPF 50

Neutrogena Invisible Daily Defense Face Mist Sunscreen Broad Spectrum SPF 50 by

Drug Labeling and Warnings

Neutrogena Invisible Daily Defense Face Mist Sunscreen Broad Spectrum SPF 50 by is a Otc medication manufactured, distributed, or labeled by Johnson & Johnson Consumer Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

NEUTROGENA INVISIBLE DAILY DEFENSE FACE MIST SUNSCREEN BROAD SPECTRUM SPF 50- 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 ® Invisible Daily defense face mist Sunscreen Broad Spectrum SPF 50

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

Flammable keep away from fire and Flame

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

  • Shake well before use.
  • 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 onto face. Spray on hands and then apply to face. Rub in.
  • Do not apply in windy conditions.
  • reapply:
    • after 40 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

SD Alcohol 40-B, Dimethicone, Trisiloxane, Diisopropyl Adipate, Acrylates/Octylacrylamide Copolymer, Acrylates/Dimethicone Copolymer, Tocopheryl Acetate, Fragrance, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice

Questions?

Call toll-free 800-299-4786 or 215-273-8755 (collect) or visit www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 100 mL Bottle Label

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Invisible Daily

defense

face mist

sunscreen

BROAD SPECTRUM

SPF 50

50

sun + antioxidants

oxybenzone free

water resistant (40 minutes)

3.4 FL OZ (100 mL)

Ntg_001

NEUTROGENA INVISIBLE DAILY DEFENSE FACE MIST SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, and octocrylene spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69968-0685
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
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
DIISOPROPYL ADIPATE (UNII: P7E6YFV72X)  
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
FEVERFEW (UNII: Z64FK7P217)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69968-0685-3100 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/05/202007/15/2023
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/05/202007/15/2023
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 1/2023
Document Id: f3080b43-b10b-41a4-e053-2995a90a9419
Set id: d19bc581-5cf9-44a1-95e5-72246dfa403b
Version: 6
Effective Time: 20230124