NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BROAD SPECTRUM SPF 60 PLUS- avobenzone, homosalate, octisalate, and octocrylene lotion 
Johnson & Johnson Consumer Inc.

----------

Neutrogena ® Invisible Daily defense lotion sunscreen BROAD SPECTRUM SPF 60+

Drug Facts

Active ingredientsPurpose
Avobenzone 3%Sunscreen
Homosalate 13.5%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 10%Sunscreen

Uses

Warnings

  • 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

Other information

Inactive ingredients

water, butyloctyl salicylate, glycerin, alcohol denat., silica, dimethicone, aluminum starch octenylsuccinate, polyurethane-62, phenoxyethanol, pentylene glycol, sodium acryloyldimethyltaurate/VP crosspolymer, acrylates/dimethicone copolymer, glyceryl stearate, chlorphenesin, styrene/acrylates copolymer, fragrance, menthyl lactate, tocopheryl acetate, disodium EDTA, trideceth-6, chrysanthemum parthenium (feverfew) flower/leaf/stem juice, sodium hydroxide, yellow 5, red 40

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 - 88 mL Tube Label

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Invisible Daily

defense

lotion

sunscreen

BROAD SPECTRUM SPF 60+

60+

sun + environment

oxybenzone free

water resistant (80 minutes)

3.0 FL OZ (88 mL)

Nuetrogena_001

NEUTROGENA INVISIBLE DAILY DEFENSE SUNSCREEN BROAD SPECTRUM SPF 60 PLUS 
avobenzone, homosalate, octisalate, and octocrylene lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0661
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) HOMOSALATE135 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
WATER (UNII: 059QF0KO0R)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
GLYCERIN (UNII: PDC6A3C0OX)  
ALCOHOL (UNII: 3K9958V90M)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
ALUMINUM STARCH OCTENYLSUCCINATE (UNII: I9PJ0O6294)  
PHENOXYETHANOL (UNII: HIE492ZZ3T)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CHLORPHENESIN (UNII: I670DAL4SZ)  
MENTHYL LACTATE, (-)- (UNII: 2BF9E65L7I)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
EDETATE DISODIUM (UNII: 7FLD91C86K)  
TRIDECETH-6 (UNII: 3T5PCR2H0C)  
FEVERFEW (UNII: Z64FK7P217)  
SODIUM HYDROXIDE (UNII: 55X04QC32I)  
FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
FD&C RED NO. 40 (UNII: WZB9127XOA)  
POLYURETHANE-62 (UNII: TBK645J3J8)  
2-ETHYLHEXYL ACRYLATE, METHACRYLATE, METHYL METHACRYLATE, OR BUTYL METHACRYLATE/HYDROXYPROPYL DIMETHICONE COPOLYMER (30000-300000 MW) (UNII: S7ZA3CCJ4M)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0661-388 mL in 1 TUBE; Type 0: Not a Combination Product10/05/2020
2NDC:69968-0661-22 in 1 CARTON10/05/2020
288 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM02010/05/2020
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 12/2023
Document Id: 0be73cd2-3857-3b6c-e063-6294a90a05ef
Set id: 1390f863-709e-412b-9a25-b65217844e44
Version: 9
Effective Time: 20231207
 
Johnson & Johnson Consumer Inc.