Label: INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN- zinc oxide lotion lotion

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 16, 2024

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  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • ACTIVE INGREDIENTS

    Zinc Oxide 17%

  • Purpose

    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 causes by the sun
  • Warnings

    For external use only

    Do not use on damanged 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 product is swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply liberally 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.
  • Inactive ingredients

    WATER / AQUA / EAU, PROPYLHEPTYL CAPRYLATE, BUTYLOCTYL SALICYLATE, PROPANEDIOL, CAPRYLYL METHICONE, DISILOXANE, POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, POLYMETHYLSILSESQUIOXANE, POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE, DISTEARDIMONIUM HECTORITE, MAGNESIUM SULFATE, TRIETHOXYCAPRYLYLSILANE, 1,2-HEXANEDIOL, SILICA, LAURYL POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE, SYNTHETIC FLUORPHLOGOPITE, DICAPRYLYL CARBONATE, CAPRYLYL GLYCOL, GLYCERYL CAPRYLATE, CHROMIUM OXIDE GREENS (CI 77288), MICA, ETHYLHEXYLGLYCERIN, SODIUM HYALURONATE, TOCOPHEROL, SQUALANE, CERAMIDE NP, NIACINAMIDE, HYDROLYZED SODIUM HYALURONATE, PANTHENOL, BUTYLENE GLYCOL, CENTELLA ASIATICA EXTRACT, CENTELLA ASIATICA LEAF EXTRACT, SACCHAROMYCES FERMENT, CENTELLA ASIATICA ROOT EXTRACT, HYDROXYPROPYLTRIMONIUM HYALURONATE, ASIATICOSIDE, MADECASSOSIDE, HYDROLYZED HYALURONIC ACID, SODIUM ACETYLATED HYALURONATE, HYALURONIC ACID, SODIUM HYALURONATE CROSSPOLYMER, POTASSIUM HYALURONATE, ASIATIC ACID, MADECASSIC ACID

  • Other information

    Protect the product in this container from excessive heat and direct sun

  • Questions?

    support@us.amorepacific.com

  • Innisfree Daily UV Defense

    Innisfree

    DAILY

    UV DEFENSE

    MINERAL

    SUNSCREEN

    BROAD SPECTRUM

    SPF 45

    Color-correcting

    Satin Finish

    50mL 1.69Fl.Oz.

    50ml mineral

  • INGREDIENTS AND APPEARANCE
    INNISFREE DAILY UV DEFENSE MINERAL SUNSCREEN 
    zinc oxide lotion lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71220-087
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE8 g  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    CENTELLA ASIATICA ROOT (UNII: 8MXU1P42J0)  
    MADECASSOSIDE (UNII: CQ2F5O6YIY)  
    1,2-HEXANEDIOL (UNII: TR046Y3K1G)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    PROPYLHEPTYL CAPRYLATE (UNII: 991Z19V2OD)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    MAGNESIUM SULFATE, UNSPECIFIED (UNII: DE08037SAB)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    MAGNESIUM POTASSIUM ALUMINOSILICATE FLUORIDE (UNII: YK3DC63Y5M)  
    DICAPRYLYL CARBONATE (UNII: 609A3V1SUA)  
    MICA (UNII: V8A1AW0880)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    WATER (UNII: 059QF0KO0R)  
    POLYGLYCERYL-2 DIPOLYHYDROXYSTEARATE (UNII: 9229XJ4V12)  
    DISTEARDIMONIUM HECTORITE (UNII: X687XDK09L)  
    GLYCERYL CAPRYLATE (UNII: TM2TZD4G4A)  
    ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    SQUALANE (UNII: GW89575KF9)  
    CENTELLA ASIATICA LEAF (UNII: 6810070TYD)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    CHROMIC OXIDE (UNII: X5Z09SU859)  
    CERAMIDE NP (UNII: 4370DF050B)  
    NIACINAMIDE (UNII: 25X51I8RD4)  
    SACCHAROMYCES CEREVISIAE (UNII: 978D8U419H)  
    MADECASSIC ACID (UNII: M7O1N24J82)  
    SODIUM ACETYLATED HYALURONATE (UNII: WN66R7GL93)  
    CENTELLA ASIATICA TRITERPENOIDS (UNII: 4YS74Q4G4J)  
    ASIATIC ACID (UNII: 9PA5A687X5)  
    ASIATICOSIDE (UNII: PKO39VY215)  
    POLYGLYCERYL-3 POLYDIMETHYLSILOXYETHYL DIMETHICONE (4000 MPA.S) (UNII: RLA2U05Z4Q)  
    POLYMETHYLSILSESQUIOXANE (4.5 MICRONS) (UNII: 59Z907ZB69)  
    CAPRYLYL TRISILOXANE (UNII: Q95M2P1KJL)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    HEXAMETHYLDISILOXANE (UNII: D7M4659BPU)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71220-087-081 in 1 BOX02/01/2024
    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 DrugM02002/01/2024
    Labeler - Innisfree Corporation (557822425)
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