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NDC 55443-0090 Vionex

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 55443-0090?
  4. Vionex Uses
  5. Active Ingredients UNII Codes
  6. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
55443-0090
Proprietary Name:
Vionex
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Metrex Research
Labeler Code:
55443
Product Label ID:
86ef8368-867f-4cb3-b44d-21a477a08e40
Start Marketing Date: [9]
01-01-1992
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
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Product Details

What is NDC 55443-0090?

The NDC code 55443-0090 is assigned by the FDA to the product Vionex which is product labeled by Metrex Research. The product's dosage form is . The product is distributed in 2 packages with assigned NDC codes 55443-0090-1 12 bottle, plastic in 1 box / 532 ml in 1 bottle, plastic (55443-0090-2), 55443-0090-6 24 bottle, plastic in 1 box / 118 ml in 1 bottle, plastic (55443-0090-4). 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 Vionex?

Place a palmful of product in one handspread on both hands and rub into the skin until dry (1-2 minutes)place a smaller amount into one hand, spread over both hands to wrist and rub into the skin until dry (30 seconds)no rinsing or wiping is requiredOther informationstore at room temperaturefor Hospital and Professional Use Only

Which are Vionex UNII Codes?

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

What is the NDC to RxNorm Crosswalk for Vionex?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:

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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".