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Nail MD by OMG Medical Group, LLC

Medically reviewed on January 15, 2018

Dosage form: spray
Ingredients: Triclosan 20mg in 1mg, TOLNAFTATE 100mg in 1mg
Labeler: OMG Medical Group, LLC
NDC Code: 55992-717

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.

Nail MD

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

miconazole nitrate 2% USP

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 
tolnafate, triclosan spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:55992-717
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
Triclosan (TRICLOSAN) Triclosan20 mg  in 1 mg
TOLNAFTATE (TOLNAFTATE) TOLNAFTATE100 mg  in 1 mg
Inactive Ingredients
Ingredient NameStrength
ETHYLHEXYLGLYCERIN 
FUSIDIC ACID 
ISOPROPYL MYRISTATE 
PHENOXYETHANOL 
ALCOHOL 
Packaging
#Item CodePackage Description
1NDC:55992-717-01100 mg in 1 PACKAGE
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph not finalpart333A02/14/2013
Labeler - OMG Medical Group, LLC (038837214)
Establishment
NameAddressID/FEIOperations
OMG Medical Group, LLC038837214repack(55992-717)
Establishment
NameAddressID/FEIOperations
Pure Source969241041manufacture(55992-717)

 
OMG Medical Group, LLC

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Disclaimer: Every effort has been made to ensure that the information provided here is accurate, up-to-date and complete, but no guarantee is made to that effect. Drug information contained herein may be time sensitive. This information has been compiled for use by healthcare practitioners and consumers in the United States. The absence of a warning for a given drug or combination thereof in no way should be construed to indicate that the drug or combination is safe, effective or appropriate for any given patient. If you have questions about the substances you are taking, check with your doctor, nurse or pharmacist.

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