Neutrogena ® Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+

Neutrogena Invisible Daily Defense Body Sunscreen Broad Spectrum SPF 60 Plus by

Drug Labeling and Warnings

Neutrogena Invisible Daily Defense Body Sunscreen Broad Spectrum SPF 60 Plus 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 BODY SUNSCREEN BROAD SPECTRUM SPF 60 PLUS- avobenzone, homosalate, octocrylene, and octisalate 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.

----------

Neutrogena ® Invisible Daily defense body spray sunscreen BROAD SPECTRUM SPF 60+

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 out of eyes. Rinse with water to remove.
  • keep away from face to avoid breathing it

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

Warning: FLAMMABLE. Contents under pressure. Do not use near fire, heat or while smoking. Do not puncture or incinerate. Store at temperature below 120°F (48°C). Use only as directed. Intentional misuse by deliberately concentrating and inhaling the contents can be harmful or fatal.

Directions

  • shake well before and frequently during use
  • spray liberally and spread evenly by hand 15 minutes before sun exposure
  • hold container 4 to 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 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., Isobutane, Dicaprylyl Carbonate, Polyester-7, Acrylates/Octylacrylamide Copolymer, Neopentyl Glycol Diheptanoate, Fragrance, Tocopheryl Acetate, 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 - 141 g Bottle Label

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Invisible Daily

defense

body spray

sunscreen

BROAD SPECTRUM SPF 60+

60+

sun + environment

oxybenzone free

water resistant (80 minutes)

5.0 OZ (141 g)

Neutrogena_001

NEUTROGENA INVISIBLE DAILY DEFENSE BODY SUNSCREEN BROAD SPECTRUM SPF 60 PLUS 
avobenzone, homosalate, octocrylene, and octisalate spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 69968-0682
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
AVOBENZONE (UNII: G63QQF2NOX) (AVOBENZONE - UNII:G63QQF2NOX) AVOBENZONE30 mg  in 1 g
HOMOSALATE (UNII: V06SV4M95S) (HOMOSALATE - UNII:V06SV4M95S) HOMOSALATE100 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
ALCOHOL (UNII: 3K9958V90M)  
ISOBUTANE (UNII: BXR49TP611)  
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
POLYESTER-7 (UNII: 0841698D2F)  
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
FEVERFEW (UNII: Z64FK7P217)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 69968-0682-5141 g in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product10/05/202004/07/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35210/05/202004/07/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 3/2023
Document Id: f6d7244a-4b34-3bb6-e053-6394a90a46ff
Set id: eed30f85-ed72-4130-9138-88037ff73edf
Version: 6
Effective Time: 20230314