Nail MD description, usages, side effects, indications, overdosage, supplying and lots more!

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Nail MD

OMG Medical Group, LLC

Nail MD


FULL PRESCRIBING INFORMATION: CONTENTS*




FULL PRESCRIBING INFORMATION

do not use on children under two years of age except under the advce and supervision of a doctor

stop use and ask a doctor if irritation occurs, if condition worsesn, or there is not improvement within four weeks

for external use only

avoid contact with eyes, scalp, vagina, penis, scrotum and anus

do not ingest

do not use on open wounds

in case of accidental ingestion, contact a physician, emergency medical

do not use if you are known to be sensitive to any of the ingredients in this product

aqua (deionized water), biotin, dimethyl sulfone (msm), ethyoxydiglycol, ethylhexylglycerin, hydrolyzed keratin proteins, hydroxyethylcellulose, phenoxyethanol, polysorbate 20, sd alcohol 40B

Active ingredient

miconazole nitrate 2% USP

Purpose

Topical antifungal

uses

antifungal drying agent

is indicated for candida albicans, trichophyton rubrum, malassezia furfur, trichophyton mentagrophytes

as well as somegram postivie bacteria

lessens the signs of nail dystophy (nail damage caused by trauma or diseas such as fungal infection)

directions

shake well before using

clean and dry affected areas

apply twice per day or as recommended by your doctor

with the brush applicator a thin layer of the product making sure to coat both the nail and cuticle completely

other information

store at controlled room temperature 15-30 degrees celsius (59-86 degrees farenhight)

protect from heat

keep from freezing, if freezing occurs, thaw out at room temperature and shake well to mix contents back to a solution

keep this and all medications out of the reach of children

Nail MD

Nail MD

Miconazole Nitrate CREAM

Product Information

Product Type Human otc drug label Item Code (Source) NDC:55992-711
Route of Administration TOPICAL DEA Schedule

Active Ingredient/Active Moiety

Ingredient Name Basis of Strength Strength
MICONAZOLE NITRATE MICONAZOLE 200 mg

Inactive Ingredients

Ingredient Name Strength
BIOTIN
water
DIMETHYL SULFONE
BIS-ETHOXYDIGLYCOL SUCCINATE
ETHYLHEXYLGLYCERIN
HYDROXYETHYL CELLULOSE (100 MPA.S AT 2%)
PHENOXYETHANOL
POLYSORBATE 20
ALCOHOL

Packaging

# Item Code Package Description Marketing Start Date Marketing End Date
1 NDC:55992-711-01 200 in 1 PACKAGE

Marketing Information

Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
partC part333C 2013-02-14


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Be sure to consult your doctor before taking any medication!
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