Label: NEUTROGENA HEALTHY DEFENSE DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 50- titanium dioxide and zinc oxide lotion

  • NDC Code(s): 69968-0515-1
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 7, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientPurpose
    Titanium Dioxide 5%Sunscreen
    Zinc Oxide 3%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 For Sunscreen Use

    • apply generously 15 minutes before sun exposure
    • reapply at least every 2 hours
    • use a water resistant sunscreen if swimming or sweating
    • 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
  • Inactive ingredients

    water, C12-15 Alkyl Benzoate, Ethylhexyl Isononanoate, Styrene/Acrylates Copolymer, Glyceryl Stearate, Glycerin, Silica, Ethylhexyl Hydroxystearate, Dimethicone, Aluminum Stearate, Cetyl Alcohol, PEG-100 Stearate, Ethylhexylglycerin, Polyhydroxystearic Acid, Phenoxyethanol, Hydroxyethyl Acrylate/Sodium Acryloyldimethyl Taurate Copolymer, PEG-75 Stearate, Pentylene Glycol, Caprylyl Glycol, Bisabolol, Isohexadecane, Chlorphenesin, Ceteth-20, Steareth-20, PPG-12/SMDI Copolymer, Disodium EDTA, Polysorbate 60, Triethoxycaprylylsilane, Dipropylene Glycol Dibenzoate, PPG-15 Stearyl Ether Benzoate, BHT, Alumina

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

    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

    pureSCREEN ®

    100% mineral actives

    SENSITIVE SKIN

    Lightweight, non-greasy, fragrance free

    Neutrogena ®

    DERMATOLOGIST RECOMMENDED

    FACIAL MOISTURIZER

    1.7 FL OZ (50mL)

    neutrogena_001

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA HEALTHY DEFENSE DAILY MOISTURIZER WITH SUNSCREEN BROAD SPECTRUM SPF 50 
    titanium dioxide and zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0515
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE50 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE30 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    ETHYLHEXYL ISONONANOATE (UNII: I6KB4GE3K4)  
    BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    ETHYLHEXYL HYDROXYSTEARATE (UNII: B7I80BVV5E)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALUMINUM STEARATE (UNII: U6XF9NP8HM)  
    CETYL ALCOHOL (UNII: 936JST6JCN)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    HYDROXYETHYL ACRYLATE/SODIUM ACRYLOYLDIMETHYL TAURATE COPOLYMER (100000 MPA.S AT 1.5%) (UNII: 86FQE96TZ4)  
    PEG-75 STEARATE (UNII: OT38R0N74H)  
    PENTYLENE GLYCOL (UNII: 50C1307PZG)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    LEVOMENOL (UNII: 24WE03BX2T)  
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    CHLORPHENESIN (UNII: I670DAL4SZ)  
    CETETH-20 (UNII: I835H2IHHX)  
    STEARETH-20 (UNII: L0Q8IK9E08)  
    PPG-12/SMDI COPOLYMER (UNII: 1BK9DDD24E)  
    EDETATE DISODIUM ANHYDROUS (UNII: 8NLQ36F6MM)  
    POLYSORBATE 60 (UNII: CAL22UVI4M)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    DIPROPYLENE GLYCOL DIBENZOATE (UNII: 6OA5ZDY41O)  
    PPG-15 STEARYL ETHER BENZOATE (UNII: 80D2J6361M)  
    BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)  
    ALUMINUM OXIDE (UNII: LMI26O6933)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0515-11 in 1 CARTON12/01/200907/20/2024
    150 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02012/01/200907/20/2024
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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