NEUTROGENA HEALTHY DEFENSE DAILY MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 50- avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion 
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 ® HEALTHY DEFENSE ® daily moisturizer with sunscreen Broad Spectrum SPF50

Drug Facts

Active ingredientsPurpose
Avobenzone 3%Sunscreen
Homosalate 12%Sunscreen
Octisalate 5%Sunscreen
Octocrylene 2.35%Sunscreen
Oxybenzone 6%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

For Sunscreen Use:

Other information

Inactive ingredients

Water, Dimethicone, Diethylhexyl 2,6-Naphthalate, Glycerin, Trisiloxane, PEG-100 Stearate, Glyceryl Stearate, Cetearyl Alcohol, Behenyl Alcohol, Potassium Cetyl Phosphate, Caprylyl Methicone, Styrene/Acrylates Copolymer, Hydrogenated Palm Glycerides, Benzyl Alcohol, Ethylhexylglycerin, Methylparaben, Cetearyl Glucoside, Xanthan Gum, Propylparaben, Tocopherol, Disodium EDTA, Polymethyl Methacrylate, BHT, Methylisothiazolinone, Tocopheryl Acetate, Ascorbic Acid, Retinyl Palmitate, Pantothenic Acid

Questions?

Call toll-free 866-638-4636 or 215-273-8755 (collect). www.neutrogena.com

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

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton

HEALTHY
DEFENSE ®

daily
moisturizer
with
sunscreen

Broad Spectrum
SPF 50

helioplex ®
broad spectrum uva•uvb

Lightweight, non-greasy moisturizer

Neutrogena ®

#1 DERMATOLOGIST RECOMMENDED
FACIAL MOISTURE

1.7 FL OZ (50mL)

PRINCIPAL DISPLAY PANEL - 50 mL Tube Carton
NEUTROGENA HEALTHY DEFENSE DAILY MOISTURIZER SUNSCREEN BROAD SPECTRUM SPF 50 
avobenzone, homosalate, octisalate, octocrylene, and oxybenzone lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0627
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) HOMOSALATE120 mg  in 1 mL
OCTISALATE (UNII: 4X49Y0596W) (OCTISALATE - UNII:4X49Y0596W) OCTISALATE50 mg  in 1 mL
OCTOCRYLENE (UNII: 5A68WGF6WM) (OCTOCRYLENE - UNII:5A68WGF6WM) OCTOCRYLENE23.5 mg  in 1 mL
OXYBENZONE (UNII: 95OOS7VE0Y) (OXYBENZONE - UNII:95OOS7VE0Y) OXYBENZONE60 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
WATER (UNII: 059QF0KO0R)  
DIMETHICONE (UNII: 92RU3N3Y1O)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
DIETHYLHEXYL 2,6-NAPHTHALATE (UNII: I0DQJ7YGXM)  
GLYCERIN (UNII: PDC6A3C0OX)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
PEG-100 STEARATE (UNII: YD01N1999R)  
CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
POTASSIUM CETYL PHOSPHATE (UNII: 03KCY6P7UT)  
DOCOSANOL (UNII: 9G1OE216XY)  
CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
PANTOTHENIC ACID (UNII: 19F5HK2737)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
TOCOPHEROL (UNII: R0ZB2556P8)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
HYDROGENATED PALM GLYCERIDES (UNII: YCZ8EM144Q)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
CETEARYL GLUCOSIDE (UNII: 09FUA47KNA)  
XANTHAN GUM (UNII: TTV12P4NEE)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
METHYLPARABEN (UNII: A2I8C7HI9T)  
PROPYLPARABEN (UNII: Z8IX2SC1OH)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0627-11 in 1 CARTON01/31/202008/02/2022
114 mL in 1 TUBE; Type 0: Not a Combination Product
2NDC:69968-0627-21 in 1 CARTON01/31/202007/20/2024
250 mL in 1 TUBE; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/31/202007/20/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 3/2023
Document Id: f6d679d0-64ba-1950-e053-6294a90a4ccc
Set id: 920bcda2-b8b1-45b6-a9d8-c4bd450bdf29
Version: 9
Effective Time: 20230314
 
Johnson & Johnson Consumer Inc.