NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BODY SPF 60 PLUS- avobenzone, homosalate, octisalate, octocrylene aerosol, spray 
Johnson & Johnson Consumer Inc.

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Neutrogena Invisible Daily Defense Sunscreen Body Spray SPF 60+

Drug Facts

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

Uses

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

Other information

Inactive ingredients

Alcohol Denat., Isobutane, Dicaprylyl Carbonate, Zingiber Officinale (Ginger) Root Extract, Tocopheryl Acetate, Polyester-7, Acrylates/Octylacrylamide Copolymer, Neopentyl Glycol Diheptanoate, Fragrance

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 Can Label

Neutrogena®

DERMATOLOGIST RECOMMENDED BRAND

Invisible Daily

defence

body spray

sunscreen

BROAD SPECTRUM SPF 60+

60+

sun + environment

oxybenzone free

water resistant (80 minutes)

NET WT. 5.0 OZ (141 g)

Neutrogena_01

NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BODY SPF 60 PLUS 
avobenzone, homosalate, octisalate, octocrylene aerosol, spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0778
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
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 g
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE100 mg  in 1 g
Inactive Ingredients
Ingredient NameStrength
DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
ALCOHOL (UNII: 3K9958V90M)  
ISOBUTANE (UNII: BXR49TP611)  
GINGER (UNII: C5529G5JPQ)  
POLYESTER-7 (UNII: 0841698D2F)  
ACRYLATE/ISOBUTYL METHACRYLATE/N-TERT-OCTYLACRYLAMIDE COPOLYMER (75000 MW) (UNII: JU3XHR8VWK)  
NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0778-5141 g in 1 CAN; Type 0: Not a Combination Product12/05/2022
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02012/05/2022
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 10/2023
Document Id: 082010ed-dbc5-21a0-e063-6294a90a0472
Set id: eaaceffa-c606-3761-e053-2995a90ae9cf
Version: 3
Effective Time: 20231020
 
Johnson & Johnson Consumer Inc.