Label: FIORE RX PIXIE DUST PINK ANTIFUNGAL NAIL POLISH- undecylenic acid film

  • 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 September 19, 2013

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

  • ACTIVE INGREDIENT

    Active Ingredient                               Purpose
    Undecylenic Acid 3%........................Anti-fungal

    Anti-fungal

  • WARNINGS

    Warnings  For external use only.
  • KEEP OUT OF REACH OF CHILDREN

    Do not use on children under 2 years of age unless directed by a doctor.

    KEEP THIS AND ALL MEDICATION OUT OF REACH OF CHILDREN.

    In case of accidental ingestion, contact a physician, emergency medical care facility or poison control center immediately for advice.

    When using this product avoid contact with eyes.

    Stop use and ask a doctor if irritation occurs.

    Directions

    Clean nails and dry thoroughly.

    Remove any nail polish with nail

    polish remover. Allow to dry

    thoroughly. Roll your bottle of Fioré

    Rx Antifungal Nail Lacquer in between

    your hands to mix the lacquer

    thoroughly. Do not shake the bottle,

    as this can introduce air bubbles that

    will affect the quality of the lacquer.

    Using only the brush provided in the

    Fioré Rx bottle, apply a strip of

    lacquer down the middle of your nail

    from cuticle to tip before following it

    with lacquer on either side. Allow

    lacquer to dry for at least 2 minutes.

    For best results, apply a second coat

    and allow to dry for 30 minutes.

    Inactive ingredients

    Butyl acetate, ethyl acetate, nitrocellulose, adipic acid/neopentyl glycol/trimellitic copolymer, acetyl tributyl citrate, isopropyl alcohol, propolis wax

    May contain:

    CI 60725, Benzophenone-3,

    Bensophenone-1, Acrylates Copolymer,

    Stearalkonium Bentonite, CI 15880, CI

    15850, Silica, N-Butyl Alcohol, CI

    15850:1, CI 77891,

    Trimethylpentanediyl Dibenzoate,

    Styrene Acrylates Copolymer,Mica, Tin

    Oxide, CI 77510, CI 19140, CI 77491

  • PRINCIPAL DISPLAY PANEL

    Back panel of bottle

  • INGREDIENTS AND APPEARANCE
    FIORE RX PIXIE DUST PINK ANTIFUNGAL NAIL POLISH 
    undecylenic acid film
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:52261-0204
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Undecylenic Acid (UNII: K3D86KJ24N) (Undecylenic Acid - UNII:K3D86KJ24N) Undecylenic Acid0.45 g  in 15 mL
    Inactive Ingredients
    Ingredient NameStrength
    Butyl Acetate (UNII: 464P5N1905) 6.2260095 g  in 15 mL
    Ethyl Acetate (UNII: 76845O8NMZ) 2.527011 g  in 15 mL
    Pyroxylin (UNII: KYR8BR2X6O) 1.979754 g  in 15 mL
    POLYESTER-10 (UNII: 212N9O2MMZ) 1.41411015 g  in 15 mL
    Acetyltributyl Citrate (UNII: 0ZBX0N59RZ) 0.98987715 g  in 15 mL
    Isopropyl Alcohol (UNII: ND2M416302) 0.84846615 mL  in 15 mL
    DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER (UNII: 905HNO1SIH) 0.141411 g  in 15 mL
    Bentoquatam (UNII: 7F465U79Q1) 0.1272684 g  in 15 mL
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.0973554 g  in 15 mL
    BUTYL ALCOHOL (UNII: 8PJ61P6TS3) 0.07071285 g  in 15 mL
    Silicon Dioxide (UNII: ETJ7Z6XBU4) 0.04242765 g  in 15 mL
    Benzoresorcinol (UNII: LJ54R4Z029) 0.02828505 g  in 15 mL
    MICA (UNII: V8A1AW0880) 0.0267153 g  in 15 mL
    PROPOLIS WAX (UNII: 6Y8XYV2NOF) 0.015 g  in 15 mL
    Trimethylpentanediyl Dibenzoate (UNII: Y8PB83G67A) 0.0141426 g  in 15 mL
    D&C RED NO. 34 (UNII: BAN556989E) 0.0007122 g  in 15 mL
    D&C RED NO. 6 (UNII: 481744AI4O) 0.00037785 g  in 15 mL
    STANNIC OXIDE (UNII: KM7N50LOS6) 0.00036345 g  in 15 mL
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:52261-0204-015 mL in 1 BOTTLE, WITH APPLICATOR
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalpart333C05/21/2013
    Labeler - Cosco International, Inc. (016433141)
    Registrant - Cosco International, Inc. (016433141)
    Establishment
    NameAddressID/FEIBusiness Operations
    Cosco International, Inc.016433141manufacture(52261-0204) , label(52261-0204) , pack(52261-0204)