Label: CLEARCHOICE SPORT SHIELD- zinc oxide lotion

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

Drug Label Information

Updated October 23, 2023

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  • Active Ingredient

    Zinc Oxide 12%

  • 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 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 the 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 10a.m.-2p.m.
    • wear long-sleeved shirts, pants, hats, and sunglasses
    • children under 6 months of age: Ask a doctor
  • Other Information

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

    Organic Aloe Vera, Thioctic Acid, Magnesium Ascorbyl Phosphate, Panthenol, Dexpanthenol, Tocopheryl Acetate, Ergocalciferol, Grape Seed Extract, Evening Primrose Oil, Sunflower Seed Oil, Safflower Seed Oil, Slippery Elm Extract, Borage Seed Oil, Alpha Bisabolol, Plantain, Allantoin, Hyaluronic Acid, Olive Squalane.

  • ClearChoice Sunscreen Tube Label (83722-000-00)

    ClearChoice Sunscreen Tube Label

  • INGREDIENTS AND APPEARANCE
    CLEARCHOICE SPORT SHIELD 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83722-000
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC CATION120 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALOE VERA WHOLE (UNII: KIZ4X2EHYX)  
    ALPHA LIPOIC ACID (UNII: 73Y7P0K73Y)  
    MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
    PANTHENOL (UNII: WV9CM0O67Z)  
    DEXPANTHENOL (UNII: 1O6C93RI7Z)  
    .ALPHA.-TOCOPHEROL ACETATE, DL- (UNII: WR1WPI7EW8)  
    ERGOCALCIFEROL (UNII: VS041H42XC)  
    VITIS VINIFERA SEED (UNII: C34U15ICXA)  
    EVENING PRIMROSE OIL (UNII: 3Q9L08K71N)  
    SUNFLOWER OIL (UNII: 3W1JG795YI)  
    SAFFLOWER SEED OIL POLYGLYCERYL-6 ESTERS (UNII: R2Z4507WJN)  
    BORAGE SEED OIL (UNII: F8XAG1755S)  
    .ALPHA.-BISABOLOL, (+/-)- (UNII: 36HQN158VC)  
    MUSA X PARADISIACA LEAF (UNII: 2UIJ27N6ED)  
    ALLANTOIN (UNII: 344S277G0Z)  
    HYALURONIC ACID (UNII: S270N0TRQY)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83722-000-00120 mL in 1 TUBE; Type 0: Not a Combination Product10/16/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02010/16/2023
    Labeler - Dermastart Inc. (146909283)
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