Fiore Rx CranApple Crush Antifungal Nail Polish description, usages, side effects, indications, overdosage, supplying and lots more!

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Fiore Rx CranApple Crush 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-fungalWarnings  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.

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.

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

Stearalkonium Bentonite, Acrylates Copolymer, CI 77891, Styrene Acrylates Copolymer, CI 15850, Silica, Benzophenone-1, Trimethylpantanediyl Dibenzoate, Mica, Tin Oxide, CI 77510, CI 19140, CI 77491

Fiore Rx CranApple Crush Antifungal Nail Polish

Fiore Rx CranApple Crush Antifungal Nail Polish

Undecylenic Acid FILM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:52261-0206
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
D&C RED NO. 7
BUTYL ALCOHOL
SILICON DIOXIDE
D&C RED NO. 6
Benzoresorcinol
PROPOLIS WAX
Trimethylpentanediyl Dibenzoate
D&C Red No. 34

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:52261-0206-0 15 in 1 BOTTLE, WITH APPLICATOR

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2013-05-22


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Be sure to consult your doctor before taking any medication!
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