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NDC 55443-0200 Vionexus

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55443-0200?
  4. Vionexus Uses
  5. Active 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:
55443-0200
Proprietary Name:
Vionexus
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Metrex Research
Labeler Code:
55443
Product Label ID:
9278a491-bddb-48da-bfb3-55d1819af381
Start Marketing Date: [9]
01-01-1992
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Navigator:

Code Structure Chart

Product Details

What is NDC 55443-0200?

The NDC code 55443-0200 is assigned by the FDA to the product Vionexus which is product labeled by Metrex Research. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 55443-0200-4 3 box in 1 case / 2 bottle, plastic in 1 box (55443-0200-3) / 1000 ml in 1 bottle, plastic (55443-0200-2), 55443-0200-5 48 bottle, plastic in 1 case / 59 ml in 1 bottle, plastic (55443-0200-1). 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 Vionexus?

Wet hands thoroughly with spray, covering entire surface of hands, including fingertips and cuticlesrub vigorously into skin until dryno rinsing or wiping is requiredOther informationstore in a dry, cool place below 104 Frecommended for use in the VioNexus No-Touch Dispenserfor hospital and professional use only

Which are Vionexus UNII Codes?

The UNII codes for the active 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".