Label: DR. MERCOLA SUNSCREEN SPF-50- titanium dioxide, zinc oxide cream

  • Category: HUMAN OTC DRUG LABEL

Drug Label Information

Updated November 10, 2023

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  • DR. MERCOLA Sunscreen SPF-50


  • ACTIVE INGREDIENT

    Titanium Dioxide (6.0%) Zinc Oxide (22.5%)

    Sunscreen

  • Uses

    • Helps prevent sunburn
    • If used as directed with other sun protection measures (see Directions), sunscreen 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 product is swallowed get medical help or contact a Poison Control Center right away.

  • Directions

    • Apply liberally 15 minutes before sun exposure.
    • Children under 6 months of age: Ask a doctor.
    • 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-sleeve shirts, pants, hats, and sunglasses
    • Re-apply:
      • After 40 minutes of swimming or sweating
      • Immediately after towel drying
      • At least every 2 hours
  • Other Information

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

    Aqua, Helanthus Annuus (Sunflower) Seed Oil, Lecithin, Glycerin, Cocos Nucifera (Coconut) Oil, Butyrospermum ParkII (Shea) Butter, Camellia Sinensis Leaf Extract, Xanthan Gum, Simmonds Chinensia (Jojoba) Seed Oil, Tocopherol, Glucurolactone, Eucalyptus Globulus Leaf Oil.

  • DR. MERCOLA Sunscreen SPF-50

    Enter section text here SPF 50

  • INGREDIENTS AND APPEARANCE
    DR. MERCOLA SUNSCREEN SPF-50 
    titanium dioxide, zinc oxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:65121-886
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE60 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE225 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    COCONUT OIL (UNII: Q9L0O73W7L)  
    SHEA BUTTER (UNII: K49155WL9Y)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    JOJOBA OIL (UNII: 724GKU717M)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    GLUCONOLACTONE (UNII: WQ29KQ9POT)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:65121-886-50160 mL in 1 BOTTLE; Type 0: Not a Combination Product02/09/2017
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02004/28/2014
    Labeler - Pure Source, LLC (080354456)
    Establishment
    NameAddressID/FEIBusiness Operations
    Pure Source, LLC080354456manufacture(65121-886)
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