Label: DERMAQUEST TM SKIN THERAPY, BREATHABLE COVERAGE TM MINERAL FOUNDATION SPF-30, DERMAMINERALS TM- zinc oxide and titanium dioxide cream

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated February 23, 2011

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS: Titanium Dioxide 4.4%, Zinc Oxide 5.5%

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: Cyclopentasiloxane , Dimethicone, Dimethicone PEG-10/15 Crosspolymer, Water(Aqua), Vinyl Dimethicone Crosspolymer, Cyclomethicone, PEG/PPG-18/18 Dimethicone, Perfluorodecalin, Hydrolyzed Ceratonai Siliqua Seed Extract, Phopspholipids, Saccgaromyces Lysate Extract, Sodium PCA, PPG-12/SMDI Copolymer, Magnesium Silicate, Nylon-12, Tocopheryl Acetate, Santalum Album (Sandalwood) Extract, Phellodendron Amurense Bark Extract, Hordeum Distichon (Barley ) Extract, Sodium Hyaluronate, Saccaromyces, Xylinium Black Tea Ferment, Glycerin, Hydroxyethylcellulose, Algae Extract, Artemesia Vulgaris Extract, Centella Asiatica Extract, Cetearyl Olivate, Sorbitan Olivate, Tetrahxyldecyl Ascorbate, Polyglyceryl-3 Polydimethylsiloxyethyl Dimethicone, Hexyl Triethoxysilylethyl Polydimethylsiloxyethyl Dimethicone, Stearic Acid, Aluminum Hydroxide, Polyglyceryl-4 Isostearate, Cetyl PEG/PPG-10/1 Dimethicone, Hexyl laurate, Phenoxyethanol, Caprylyl Glycol, Ethylhexylglycerin, Hexylene Glycol, Aloe Barbedensis Leaf Juice Powder.

    [+/- (May Contain) Iron Oxides (Cl77499, Cl 77491, Cl77492), Titanium Dioxide (Cl 77891)]

  • PRINCIPAL DISPLAY PANEL



    DIRECTIONS:

    Apply with a foundation brush for flawless coverage. Discontinue use if irritation develops.

    Protect from harmful UVA and UVB rays while creating the perfect canvas with our mineral-based SPF 30 liquid foundation.

    Paraben-Free

    Talc-Free

    SyntheticDye-Free

    Bismuth Oxychloride-Free

    Oil-Free

    Very WaterResistant          


    Manufactured for DermaQuest TM, Inc.

    Hayward

    CA, 94544

    dermaquestinc.com

    Made in USA


    PRINCIPAL DISPLAY PANEL:

    DERMAQUEST SKIN THERAPY

    Breathable Coverage

    Mineral Foundation SPF30

    DermaMinerals TM

    1 Fl Oz / 29.6 mL

    Image of Principal Display Panel


      


  • INGREDIENTS AND APPEARANCE
    DERMAQUEST TM SKIN THERAPY, BREATHABLE COVERAGE TM MINERAL FOUNDATION SPF-30, DERMAMINERALS TM 
    zinc oxide and titanium dioxide cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62742-4030
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) (Titanium - UNII:D1JT611TNE) TITANIUM DIOXIDE48 mg  in 1 mL
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC CATION - UNII:13S1S8SF37) ZINC OXIDE58 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Dimethicone (UNII: 92RU3N3Y1O)  
    Water (UNII: 059QF0KO0R)  
    Cyclomethicone (UNII: NMQ347994Z)  
    HYALURONATE SODIUM (UNII: YSE9PPT4TH)  
    HYDROXYETHYL CELLULOSE (2000 CPS AT 1%) (UNII: S38J6RZN16)  
    Stearic Acid (UNII: 4ELV7Z65AP)  
    Aluminum Hydroxide (UNII: 5QB0T2IUN0)  
    Hexyl Laurate (UNII: 4CG9F9W01Q)  
    Phenoxyethanol (UNII: HIE492ZZ3T)  
    Hexylene Glycol (UNII: KEH0A3F75J)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    CYCLOMETHICONE 5 (UNII: 0THT5PCI0R)  
    SODIUM PYRROLIDONE CARBOXYLATE (UNII: 469OTG57A2)  
    MAGNESIUM TRISILICATE (UNII: C2E1CI501T)  
    .ALPHA.-TOCOPHEROL ACETATE, D- (UNII: A7E6112E4N)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62742-4030-21 in 1 CARTON
    1NDC:62742-4030-130 mL in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart35210/01/2009
    Labeler - Allure Labs, Inc. (926831603)