Label: NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30- titanium dioxide, zinc oxide lotion

  • NDC Code(s): 69968-0815-1, 69968-0815-2
  • Packager: Johnson & Johnson Consumer Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENT

    Active ingredientsPurpose
    Titanium Dioxide (4.9%)Sunscreen
    Zinc Oxide (21.6%)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

    Shake bottle well before use.

    • For Sunscreen Use:

    • apply generously 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 the product from excessive heat and direct sun
    • may stain some fabrics
  • Inactive ingredients

    Water, Isononyl Isononanoate, Dicaprylyl Ether, C12-15 Alkyl Benzoate, Polyglyceryl-2 Dipolyhydroxystearate, Propylene Glycol, Dimethicone, Zingiber Officinale (Ginger) Root Extract, Tocopheryl Acetate, Chrysanthemum Parthenium (Feverfew) Flower/Leaf/Stem Juice, Calcium Sodium Borosilicate, Polyhydroxystearic Acid, Triethoxycaprylylsilane, Sorbitan Sesquioleate, Sodium Chloride, Aluminum Hydroxide, Phenoxyethanol, Triacontanyl PVP, Ethylhexylglycerin, Stearic Acid, Iron Oxides

  • 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 - 40 mL Bottle Label

    NEW

    Neutrogena®

    DERMATOLOGIST RECOMMENDED BRAND

    PURESCREEN+TM

    MINERAL

    INVISIBLE

    DAILY

    DEFENSE

    FACE LIQUID

    30

    SUNSCREEN

    BROAD SPECTRUM SPF 30

    UVA/UVB PROTECTION

    sun + environment ∙ invisible finish

    antioxidant complex ∙ oxybenzone free

    water resistant (80 minutes)

    1.4 FL OZ (40 mL)

    Neutrogena_01

  • INGREDIENTS AND APPEARANCE
    NEUTROGENA MINERAL INVISIBLE DAILY DEFENSE FACE SUNSCREEN BROAD SPECTRUM SPF 30 
    titanium dioxide, zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:69968-0815
    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 OXIDE216 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    SORBITAN SESQUIOLEATE (UNII: 0W8RRI5W5A)  
    ALKYL (C12-15) BENZOATE (UNII: A9EJ3J61HQ)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    GINGER (UNII: C5529G5JPQ)  
    .ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    TRIACONTANYL PVP (WP-660) (UNII: N0SS3Q238D)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    FERROUS OXIDE (UNII: G7036X8B5H)  
    FEVERFEW (UNII: Z64FK7P217)  
    ISONONYL ISONONANOATE (UNII: S4V5BS6GCX)  
    DICAPRYLYL ETHER (UNII: 77JZM5516Z)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:69968-0815-11 in 1 CARTON08/21/2023
    140 mL in 1 BOTTLE; Type 0: Not a Combination Product
    2NDC:69968-0815-224 in 1 TRAY01/01/2024
    21.4 mL in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02008/21/2023
    Labeler - Johnson & Johnson Consumer Inc. (118772437)
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