Label: NEUTROGENA ULTRA SHEER DRY-TOUCH SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide, zinc oxide lotion

  • NDC Code(s): 69968-0892-1, 69968-0892-3
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated May 20, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Titanium Dioxide (6.6%), Zinc Oxide (18.0%)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 liberally 15 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, Isohexadecane, Butyloctyl Salicylate, C12-15 Alkyl Benzoate, Dimethicone, Ethylhexyl methoxycrylene, Caprylyl Methicone, Glyceryl Stearate, PEG-100 Stearate, Calcium Sodium Borosilicate, VP/Hexadecene Copolymer, Styrene/Acrylates Copolymer, Triethoxycaprylylsilane, Aluminum Hydroxide, Xanthan Gum, Stearic Acid, Trisiloxane, Polyester-7, Phenoxyethanol, Polyhydroxystearic Acid, Caprylyl Glycol, Ethylhexylglycerin, Neopentyl Glycol Diheptanoate, Behenyl Alcohol, Tocopheryl Acetate, Disodium EDTA, Silica

  • Questions?

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

  • SPL UNCLASSIFIED SECTION

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

  • PRINCIPAL DISPLAY PANEL - 88 mL Tube Label

    NEW LOOK

    Neutrogena ®

    DERMATOLOGIST RECOMMENDED BRAND

    ULTRA

    SHEER ®

    Dry-Touch

    Sunscreen

    MINERAL SENSITIVE SKIN

    30

    BROAD SPECTRUM SPF 30

    Antioxidant Vitamin E

    100% Mineral Actives

    Lightweight clean feel

    with PURESCREEN+®

    Water resistant (80 minutes)

    3.0 FL OZ (88 mL)

    69968-0892-1

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA ULTRA SHEER DRY-TOUCH SUNSCREEN BROAD SPECTRUM SPF 30 
    titanium dioxide, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0892
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE180 mg  in 1 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE66 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISOHEXADECANE (UNII: 918X1OUF1E)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    NEOPENTYL GLYCOL DIHEPTANOATE (UNII: 5LKW3C543X)  
    ETHYLHEXYL METHOXYCRYLENE (UNII: S3KFG6Q5X8)  
    VINYLPYRROLIDONE/HEXADECENE COPOLYMER (UNII: KFR5QEN0N9)  
    BUTYL METHACRYLATE/METHYL METHACRYLATE/METHACRYLIC ACID/STYRENE CROSSPOLYMER (UNII: V5RS026Q0H)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    DOCOSANOL (UNII: 9G1OE216XY)  
    ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    WATER (UNII: 059QF0KO0R)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    TRISILOXANE (UNII: 9G1ZW13R0G)  
    PEG-100 STEARATE (UNII: YD01N1999R)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POLYESTER-7 (UNII: 0841698D2F)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0892-388 mL in 1 TUBE; Type 0: Not a Combination Product07/01/2024
    2NDC:69968-0892-112 in 1 TRAY07/01/2024
    214 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02007/01/2024
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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