Label: IASO COVER VEIL PACT 25- zinc oxide powder

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 March 2, 2018

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  • ACTIVE INGREDIENT

    zinc oxide


  • INACTIVE INGREDIENT

    mica, talc, titanium dioxide, silica, dimethicone, methyl methacrylate crosspolymer, nylon-12, zinc oxide, ci 77492, phenyl trimethicone, chitosan, lauroyl lysine, squalane, triethylhexanoin, trifluoromethyl c1-4 alkyl dimethicone, aluminum dimyristate, c9-15 fluoroalcohol phosphate, methicone, ci 77491, ci 77499, hydrogenated lecithin, aluminum hydroxide, disodium stearoyl glutamate, methylparaben, fragrance, carnauba wax, propylparaben, stearyl glycyrrhetinate, trimethylsiloxysilicate, alumina, camellia sinensis leaf ext, citrus unshiu fruit oil, tocopheryl acetate, glycerin water, butylene glycol, carbomer, polysorbate 20, palmitoyl pentapeptide-4


  • PURPOSE

    skin protectant


  • KEEP OUT OF REACH OF CHILDREN

    keep out of reach of the children

  • INDICATIONS & USAGE

    using a regular powder puff for the natural look and soft matte finish
    apply the powder to the entire face, moving inside to the facial line
    using a sponge powder puff for high coverage and smooth finish
    blend the powder on to the entire face, moving outward to the facial line


  • WARNINGS

    - Stop using if sensitivities occurs and consult with dermatologist
    - sensitivities such as red marks, intumescence, urtication, irritation during use
    -Have sensitivities as above on applied part by direct sun ray
    - Do not store at high and low temperatures and avoid sunlight.


  • DOSAGE & ADMINISTRATION

    for external use only

  • PRINCIPAL DISPLAY PANEL

    package label
  • INGREDIENTS AND APPEARANCE
    IASO COVER VEIL PACT 25 
    zinc oxide powder
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:75847-1710
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ZINC OXIDE (UNII: SOI2LOH54Z) (ZINC OXIDE - UNII:SOI2LOH54Z) ZINC OXIDE0.0192 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    DIMETHICONE (UNII: 92RU3N3Y1O)  
    ALUMINUM HYDROXIDE (UNII: 5QB0T2IUN0)  
    SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
    SQUALENE (UNII: 7QWM220FJH)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:75847-1710-114 g in 1 PACKAGE; Type 0: Not a Combination Product03/12/2018
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart34708/01/2013
    Labeler - IASO Inc (688771690)
    Registrant - IASO Inc (688771690)
    Establishment
    NameAddressID/FEIBusiness Operations
    Kolmar Korea Co., Ltd689847167manufacture(75847-1710)
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