NDC 55992-717

Nail MD

Tolnafate, Triclosan

Nail MD is a Topical Spray in the Human Otc Drug category. It is labeled and distributed by Omg Medical Group, Llc. The primary component is Triclosan; Tolnaftate.

• Product ID: 55992-717_83fb189b-4b17-42e9-b8f6-6ba95ac31796
• NDC: 55992-717
• Product Type: Human Otc Drug
• Proprietary Name: Nail MD
• Generic Name: Tolnafate, Triclosan
• Dosage Form: Spray
• Route of Administration: TOPICAL
• Marketing Start Date: 2013-02-14
• Marketing Category: OTC MONOGRAPH NOT FINAL / OTC MONOGRAPH NOT FINAL
• Application Number: part333A
• Labeler Name: OMG Medical Group, LLC
• Substance Name: TRICLOSAN; TOLNAFTATE
• Active Ingredient Strength: 20 mg/mg; mg/mg
• NDC Exclude Flag: E
• Listing Certified Through: 2017-12-31

Packaging

NDC 55992-717-01

100 mg in 1 PACKAGE (55992-717-01)

• Marketing Start Date: 2013-02-14
• NDC Exclude Flag: N
• Sample Package?: N

NDC SPL Data Element Entries

NDC 55992-717-01 [55992071701]

Nail MD SPRAY

• Marketing Category: OTC monograph not final
• Application Number: part333A
• Product Type: HUMAN OTC DRUG
• Marketing Start Date: 2013-02-14
• Inactivation Date: 2019-11-27

Drug Details

Active Ingredients

Ingredient	Strength
TRICLOSAN	20 mg/mg

OpenFDA Data

• SPL SET ID: ee7522ab-7d4d-4370-a78f-03c9955734e7
• Manufacturer:
  • OMG Medical Group, LLC
• UNII:
  • 4NM5039Y5X
  • 06KB629TKV
• RxNorm Concept Unique ID - RxCUI:
  • 1486762
  • 1486787

NDC Crossover Matching brand name "Nail MD" or generic name "Tolnafate, Triclosan"

NDC	Brand Name	Generic Name
55992-711	Nail MD	Miconazole Nitrate
55992-717	Nail MD	Tolnafate, Triclosan