Label: MINERAL LP FOUNDATION VANILLA- mineral lp foundation cream

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

Drug Label Information

Updated April 22, 2024

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  • Actives

    Titanium Dioxide 6%

    Zinc Oxide 3%

  • Purpose

    Sunscreen

  • 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. Stop use and ask doctor if rash occurs.

  • INDICATIONS & USAGE

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

  • 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.

  • Directions

    Apply liberally 15 minutes before sun exposure. Use a 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 a.m. - 2:00 p.m. Wear long sleeved shirts, pants, hats, and sunglasses.

  • Inactive Ingredients

    Cyclopentasiloxane, Aqua/Water/Eau, Dimethicone Crosspolymer, Octyldodecyl Neopentanoate, Butylene Glycol, Cetyl PEG/PPG-10/1 Dimethicone, Polyglyceryl-4 Isostearate, Aluminum Hydroxide, Stearic Acid, Dimethicone, Hexyl Laurate, Silica, Tocopherol, Tetrahexyldecyl Ascorbate, Sodium Hyaluronate, PEG/PPG-18/18 Dimethicone, Phytantriol, Nylon-12, Sodium Chloride, Nylon-12 Fluorescent Brightener 230 Salt, Polyvinylalcohol Crosspolymer, Octyldodecanol, Magnesium Chloride, Potassium Chloride, Zinc Chloride , Lysine, Methicone, Triethoxycaprylylsilane, Disodium EDTA, Hexylene Glycol, Caprylyl Glycol, Phenoxyethanol, Potassium Sorbate,Mica ,Titanium Dioxide (CI 77891), Iron Oxides (CI 77492), Iron Oxides (CI 77491), Iron Oxides (CI 77499)

  • Other Information

    Protect this product from excessive heat and direct sun

  • PRINCIPAL DISPLAY PANEL

    Mineral Liquid Powder Fondation (LPMF)ML Label

  • INGREDIENTS AND APPEARANCE
    MINERAL LP FOUNDATION VANILLA 
    mineral lp foundation cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84179-207
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE3 g  in 30 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (TITANIUM DIOXIDE - UNII:15FIX9V2JP) TITANIUM DIOXIDE6 g  in 30 mL
    Inactive Ingredients
    Ingredient NameStrength
    FERRIC OXIDE YELLOW (UNII: EX438O2MRT)  
    FERROSOFERRIC OXIDE (UNII: XM0M87F357)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    POTASSIUM CHLORIDE (UNII: 660YQ98I10)  
    OCTYLDODECYL NEOPENTANOATE (UNII: X8725R883T)  
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    DISODIUM 4,4'-BIS((4-ANILINO-6-((2-CARBAMOYLETHYL)(2-HYDROXYETHYL)AMINO)-S-TRIAZIN-2-YL)AMINO)-2,2'-STILBENEDISULFONATE (UNII: 30I2S866LK)  
    MICA (UNII: V8A1AW0880)  
    FERRIC OXIDE RED (UNII: 1K09F3G675)  
    POTASSIUM SORBATE (UNII: 1VPU26JZZ4)  
    POLYVINYL ALCOHOL, UNSPECIFIED (UNII: 532B59J990)  
    MAGNESIUM CHLORIDE (UNII: 02F3473H9O)  
    ZINC CHLORIDE (UNII: 86Q357L16B)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    LYSINE (UNII: K3Z4F929H6)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    POLYGLYCERYL-4 ISOSTEARATE (UNII: 820DPX33S7)  
    WATER (UNII: 059QF0KO0R)  
    HEXYL LAURATE (UNII: 4CG9F9W01Q)  
    DIMETHICONE CROSSPOLYMER (450000 MPA.S AT 12% IN CYCLOPENTASILOXANE) (UNII: UF7620L1W6)  
    METHICONE (20 CST) (UNII: 6777U11MKT)  
    TRIETHOXYCAPRYLYLSILANE (UNII: LDC331P08E)  
    CAPRYLYL GLYCOL (UNII: 00YIU5438U)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    STEARIC ACID (UNII: 4ELV7Z65AP)  
    TETRAHEXYLDECYL ASCORBATE (UNII: 9LBV3F07AZ)  
    PEG/PPG-18/18 DIMETHICONE (UNII: 9H0AO7T794)  
    NYLON-12 (UNII: 446U8J075B)  
    CETYL PEG/PPG-10/1 DIMETHICONE (HLB 3) (UNII: G300307ZXP)  
    TOCOPHEROL (UNII: R0ZB2556P8)  
    PHYTANTRIOL (UNII: 8LVI07A72W)  
    OCTYLDODECANOL (UNII: 461N1O614Y)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    HEXYLENE GLYCOL (UNII: KEH0A3F75J)  
    Product Characteristics
    ColorbrownScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84179-207-011 in 1 CARTON08/01/2011
    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 DrugM02008/01/2011
    Labeler - JENTRY KELLEY (040036679)
    Registrant - MANA Products, Inc. (078870292)
    Establishment
    NameAddressID/FEIBusiness Operations
    MANA Products, Inc078870292manufacture(84179-207)
    Establishment
    NameAddressID/FEIBusiness Operations
    MANA Products,Inc032870270manufacture(84179-207)
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