NEUTROGENA SENSITIVE SKIN MINERAL SUNSCREEN BROAD SPECTRUM SPF 60 PLUS- titanium dioxide and zinc oxide 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 ® Sensitive Skin mineral sunscreen BROAD SPECTRUM SPF 60+

Drug Facts

Active ingredientsPurpose
Titanium Dioxide (4.9%)Sunscreen
Zinc Oxide (4.7%)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.

  • 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

  • apply generously and evenly15 minutes before sun exposure
  • 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

Water, Butyloctyl Salicylate, Beeswax, Styrene/Acrylates Copolymer, Silica, PEG-8, Butylene Glycol, PEG-100 Stearate, Glyceryl Stearate, Cetyl Dimethicone, Benzyl Alcohol, Dimethicone, Methicone, Arachidyl Alcohol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, Polyhydroxystearic Acid, Xanthan Gum, Isohexadecane, Behenyl Alcohol, Trisiloxane, Ethylhexylglycerin, Disodium EDTA, Trimethylsiloxysilicate, Arachidyl Glucoside, Bisabolol, Dipotassium Glycyrrhizate, Triethoxycaprylylsilane, Polysorbate 60, BHT, Stearic Acid, Methylisothiazolinone, Polyaminopropyl Biguanide, Polymethyl Methacrylate, Tocopheryl Acetate, Retinyl Palmitate, Ascorbic Acid, Pantothenic Acid, Alumina

Questions?

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

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

PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

Neutrogena ®

DERMATOLOGIST RECOMMENDED BRAND

Sensitive

Skin

mineral sunscreen

BROAD SPECTRUM SPF 60+

60+

100% mineral actives

water resistant (80 minutes)

3.0 FL OZ (88mL)

Neutrogena_001

NEUTROGENA SENSITIVE SKIN MINERAL SUNSCREEN BROAD SPECTRUM SPF 60 PLUS 
titanium dioxide and zinc oxide lotion
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0619
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE49 mg  in 1 mL
ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE47 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
DIMETHICONE (UNII: 92RU3N3Y1O)  
METHICONE (20 CST) (UNII: 6777U11MKT)  
ARACHIDYL ALCOHOL (UNII: 1QR1QRA9BU)  
HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
XANTHAN GUM (UNII: TTV12P4NEE)  
ISOHEXADECANE (UNII: 918X1OUF1E)  
DOCOSANOL (UNII: 9G1OE216XY)  
WATER (UNII: 059QF0KO0R)  
BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
YELLOW WAX (UNII: 2ZA36H0S2V)  
BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
PEG-100 STEARATE (UNII: YD01N1999R)  
GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
CETYL DIMETHICONE 25 (UNII: U4AS1BW4ZB)  
BENZYL ALCOHOL (UNII: LKG8494WBH)  
TRISILOXANE (UNII: 9G1ZW13R0G)  
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
ARACHIDYL GLUCOSIDE (UNII: 6JVW35JOOJ)  
LEVOMENOL (UNII: 24WE03BX2T)  
GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)  
TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
POLYSORBATE 60 (UNII: CAL22UVI4M)  
BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
STEARIC ACID (UNII: 4ELV7Z65AP)  
METHYLISOTHIAZOLINONE (UNII: 229D0E1QFA)  
POLYAMINOPROPYL BIGUANIDE (UNII: DT9D8Z79ET)  
POLY(METHYL METHACRYLATE; 450000 MW) (UNII: Z47NNT4J11)  
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
ASCORBIC ACID (UNII: PQ6CK8PD0R)  
PANTOTHENIC ACID (UNII: 19F5HK2737)  
ALUMINUM OXIDE (UNII: LMI26O6933)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:69968-0619-388 mL in 1 TUBE; Type 0: Not a Combination Product01/31/202004/29/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart35201/31/202004/29/2024
Labeler - Johnson & Johnson Consumer Inc. (118772437)

Revised: 3/2023
Document Id: f78d1ce3-1d90-c377-e053-6394a90af787
Set id: 0d621501-7884-460a-ab69-37f8d6d0b5ba
Version: 8
Effective Time: 20230323
 
Johnson & Johnson Consumer Inc.