Fiore Rx Eggplant My Garden Antifungal Nail Polish description, usages, side effects, indications, overdosage, supplying and lots more!

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Fiore Rx Eggplant My Garden 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 anhydride, 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 Eggplant My Garden Antifungal Nail Polish

Fiore Rx Eggplant My Garden Antifungal Nail Polish

Undecylenic Acid FILM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52261-0205
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
BENTOQUATAM
DIMETHYLAMINOETHYL METHACRYLATE - BUTYL METHACRYLATE - METHYL METHACRYLATE COPOLYMER
POLACRILIN
D&C Red No. 34
titanium dioxide
FERRIC AMMONIUM FERROCYANIDE
SILICON DIOXIDE
Benzoresorcinol
PROPOLIS WAX
Trimethylpentanediyl Dibenzoate
FD&C YELLOW NO. 5
D&C RED NO. 6

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52261-0205-0 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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Be sure to consult your doctor before taking any medication!
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