Fiore Rx Pixie Dust Pink Antifungal Nail Polish description, usages, side effects, indications, overdosage, supplying and lots more!

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Fiore Rx Pixie Dust Pink Antifungal Nail Polish

Cosco International, Inc.
Cosco International, Inc.

Drug Facts




FULL PRESCRIBING INFORMATION

Active ingredient

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

Purpose

Anti-fungal

Warnings  For external use only.

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.

Uses

When using this product avoid contact with eyes.

Stop use and ask a doctor if irritation occurs.

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.

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

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

Fiore Rx Pixie Dust Pink Antifungal Nail Polish

Fiore Rx Pixie Dust Pink Antifungal Nail Polish

Undecylenic Acid FILM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52261-0204
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
UNDECYLENIC ACID 0.45 g

Inactive Ingredients

Ingredient Name Strength
BUTYL ACETATE
ETHYL ACETATE
PYROXYLIN
POLYESTER-10
ACETYLTRIBUTYL CITRATE
ISOPROPYL ALCOHOL
DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER
BENTOQUATAM
titanium dioxide
BUTYL ALCOHOL
SILICON DIOXIDE
Benzoresorcinol
MICA
PROPOLIS WAX
Trimethylpentanediyl Dibenzoate
D&C Red No. 34
D&C RED NO. 6
STANNIC OXIDE

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52261-0204-0 15 in 1 BOTTLE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2013-05-21


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