Label: MINERAL SHEER SCREEN BROAD SPECTRUM SUNSCREEN SPF 30- zinc oxide lotion

  • NDC Code(s): 75936-305-01, 75936-305-02, 75936-305-03, 75936-305-04, view more
    75936-305-05
  • Packager: Supergoop LLC
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 16, 2024

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  • ACTIVE INGREDIENT

    Active Ingredient Purpose

    Zinc Oxide 17.5% Sunscreen

  • PURPOSE

    Sunscreen

    Helps prevent sunburn.

    If used as directed with other sun protection measures (see Directions), decreases the risk of skin cancer and early skin againg caused by the sun.

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    Stop use and ask a doctor if rash occurs.

  • WARNINGS

    For external use only

    Do not use on damaged or broken skin

    When using this product kee out of eyes. Rinse with water to remove.

  • DOSAGE & ADMINISTRATION

    • apply generously and evenly 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 sunglassess
    • Children under 6 months: Ask a doctor.

  • INACTIVE INGREDIENT

    Water, Isododecane, Caprylic/Capric Triglyceride, Butyloctyl Salicylate, Propanedlol, Glycerin, Squalane, Trioctyldodecyl Citrate, Polyglycerln-3, Polyglyceryl-3 Lactate/Laurate, Polysilicone-11, Cetearyl Alcohol, Glyceryl Stearate, Sodium Stearoyl Glutamate, Butylene Glycol, Xanthan Gum, Polyacrylate Crosspolymer-6, lsostearic Acid, Lecithin, Polyglyceryl-3 Polyricinoleate, Polyhydroxystearic Acid, Caprylhydroxamic Acid, Citric Acid, Aloe Barbadensis Leaf Juice, Lespedeza Capitata Leaf/Stem Extract, Maltodextrin, Sodium Hyaluronate

  • STORAGE AND HANDLING

    Protect the product In this container from excessive heat and direct sun.

  • PRINCIPAL DISPLAY PANEL

    Mineral Sheer Screen

    SPF 30

    100% Mineral

    Broad Spectrum Sunscreen

    SPF 30 PA+++

    1.5 fl. oz./45 ml

    CartonTube

  • INGREDIENTS AND APPEARANCE
    MINERAL SHEER SCREEN BROAD SPECTRUM SUNSCREEN SPF 30 
    zinc oxide lotion
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75936-305
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE17.5 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    ISODODECANE (UNII: A8289P68Y2)  
    MEDIUM-CHAIN TRIGLYCERIDES (UNII: C9H2L21V7U)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    TRIOCTYLDODECYL CITRATE (UNII: 35X8CT063R)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    POLYGLYCERYL-3 PENTARICINOLEATE (UNII: 7Q0OK5DOT4)  
    POLYHYDROXYSTEARIC ACID (2300 MW) (UNII: YXH47AOU0F)  
    CAPRYLHYDROXAMIC ACID (UNII: UPY805K99W)  
    AMMONIUM ACRYLOYLDIMETHYLTAURATE, DIMETHYLACRYLAMIDE, LAURYL METHACRYLATE AND LAURETH-4 METHACRYLATE COPOLYMER, TRIMETHYLOLPROPANE TRIACRYLATE CROSSLINKED (45000 MPA.S) (UNII: Q7UI015FF9)  
    SODIUM STEAROYL GLUTAMATE (UNII: 65A9F4P024)  
    POLYGLYCERIN-3 (UNII: 4A0NCJ6RD6)  
    DIMETHICONE/VINYL DIMETHICONE CROSSPOLYMER (SOFT PARTICLE) (UNII: 9E4CO0W6C5)  
    ALOE VERA LEAF (UNII: ZY81Z83H0X)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    BUTYLOCTYL SALICYLATE (UNII: 2EH13UN8D3)  
    PROPANEDIOL (UNII: 5965N8W85T)  
    SQUALANE (UNII: GW89575KF9)  
    ISOSTEARIC ACID (UNII: X33R8U0062)  
    LECITHIN, SOYBEAN (UNII: 1DI56QDM62)  
    CETOSTEARYL ALCOHOL (UNII: 2DMT128M1S)  
    XANTHAN GUM (UNII: TTV12P4NEE)  
    CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)  
    MALTODEXTRIN (UNII: 7CVR7L4A2D)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75936-305-0145 mL in 1 TUBE; Type 0: Not a Combination Product01/12/2021
    2NDC:75936-305-0215 mL in 1 TUBE; Type 0: Not a Combination Product01/12/2021
    3NDC:75936-305-0310 mL in 1 TUBE; Type 0: Not a Combination Product01/12/2021
    4NDC:75936-305-045 mL in 1 TUBE; Type 0: Not a Combination Product01/12/2021
    5NDC:75936-305-0520 mL in 1 TUBE; Type 0: Not a Combination Product08/26/2021
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02001/12/2021
    Labeler - Supergoop LLC (117061743)
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