Label: YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20-ALMOND- your name mineral sheer tint cream

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

Drug Label Information

Updated January 4, 2024

If you are a consumer or patient please visit this version.

  • ACTIVE INGREDIENTS

    Titanium Dioxide 5.00%

    Zinc Oxide 5.00%

  • PURPOSE

    Sunscreen active

  • USE

    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.
  • DIRECTIONS

    Apply liberally 15 minutes before sun exposure.
    Use water resistant sunscreen if swimming or sweating.

    Reapply at least every 2 hours.

    Children under 6 months: ask a doctor.
    Sun Protection Measures: Spending time in the sun increases risk of skin cancer and early 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 10:00 am - 2:00 pm. Wear long sleeved shirts, pants, hats and sunglasses.

  • OTHER INFORMATION

    PDPProtect this product from exessive heat and direct sun.

  • INDICATIONS & USAGE

    Stop use and ask a doctor if rash occurs.

  • INACTIVE INGREDIENT

    Water, Cyclopentasiloxane, Butylene Glycol, Titanium Dioxide, Zinc Oxide, Octyldodecyl Neopentanoate, PEG/PPG-18/18 Dimethicone, Dimethicone, Tocopherol, Tetrahexyldecyl Ascorbate, Retinyl Palmitate, Camellia Sinensis Leaf Extract, Chamomilla Recutita (Matricaria) Flower Extract, Ginkgo Biloba Leaf Extract, Panax Ginseng Root Extract, Octyldodecanol, Boron Nitride, Dextrin Palmitate, Palmitic Acid, Methicone, Stearic Acid, Magnesium Chloride, Potassium Chloride, Sodium Chloride, Zinc Chloride, Magnesium Ascorbyl Phosphate, Sodium Hyaluronate, Phytantriol, Glycerin, Triethoxycaprylylsilane, Lysine, Aluminum Hydroxide, Disodium EDTA, Hexylene Glycol, Potassium Sorbate, Sodium Dehydroacetate, Caprylyl Glycol, Phenoxyethanol

    MAY CONTAIN (+/-):

    Mica, Titanium Dioxide (CI 77891), Iron Oxides (CI 77491, CI 77492, CI 77499)

  • KEEP OUT OF REACH OF CHILDREN

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

  • PRINCIPAL DISPLAY PANEL

    Label-cartonPDP

  • INGREDIENTS AND APPEARANCE
    YOUR NAME MINERAL SHEERTINT BROAD SPECTRUM SPF 20-ALMOND 
    your name mineral sheer tint cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:59735-175
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE5 g  in 30 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE5 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    HYALURONIC ACID (NON-ANIMAL STABILIZED) (UNII: B7SG5YV2SI)  
    PHYTANTRIOL (UNII: 8LVI07A72W)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)  
    DEXTRIN PALMITATE (CORN; 20000 MW) (UNII: 89B2BSF9I3)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    LYSINE (UNII: K3Z4F929H6)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    SODIUM DEHYDROACETATE (UNII: 8W46YN971G)  
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    ASIAN GINSENG (UNII: CUQ3A77YXI)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    METHICONE (20 CST) (UNII: 6777U11MKT)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    BORON NITRIDE (UNII: 2U4T60A6YD)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    GREEN TEA LEAF (UNII: W2ZU1RY8B0)  
    CHAMOMILE (UNII: FGL3685T2X)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    MICA (UNII: V8A1AW0880)  
    PALMITIC ACID (UNII: 2V16EO95H1)  
    WATER (UNII: 059QF0KO0R)  
    GINKGO (UNII: 19FUJ2C58T)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    MAGNESIUM ASCORBYL PHOSPHATE (UNII: 0R822556M5)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:59735-175-011 in 1 CARTON02/01/2011
    130 mL in 1 TUBE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM02002/01/2011
    Labeler - Mana Product, Inc (078870292)
    Registrant - Mana Product, Inc (078870292)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mana Products,Inc032870270manufacture(59735-175)
    Establishment
    NameAddressID/FEIBusiness Operations
    Mana Products, Inc078870292manufacture(59735-175)