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  4. NDC Product Code: 82743-101 Toenail Fungus / Nail Repair Pen

NDC 82743-101 Toenail Fungus / Nail Repair Pen

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 82743-101?
  4. Toenail Fungus / Nail Repair Pen Uses
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
82743-101
Proprietary Name:
Toenail Fungus / Nail Repair Pen
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Vital Synergy Llc
Labeler Code:
82743
Product Label ID:
df28c13e-da4a-46c9-e053-2995a90a6597
Start Marketing Date: [9]
05-16-2022
Listing Expiration Date: [11]
12-31-2023
Exclude Flag: [12]
I
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Product Details

What is NDC 82743-101?

The NDC code 82743-101 is assigned by the FDA to the product Toenail Fungus / Nail Repair Pen which is product labeled by Vital Synergy Llc. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 82743-101-30 1 bottle, with applicator in 1 box / 30 ml in 1 bottle, with applicator (82743-101-01), 82743-101-63 6 bottle, with applicator in 1 box / 3 ml in 1 bottle, with applicator (82743-101-03). This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Toenail Fungus / Nail Repair Pen?

TEST ON A SMALL PART OF A NAIL FIRST. APPLY TOPICALLY TWICE PER DAY ON THE AFFECTED AREA.

Which are Toenail Fungus / Nail Repair Pen UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Toenail Fungus / Nail Repair Pen Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

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Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".