Vionexus
NDC Package 55443-0200-4

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Vionexus is 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. Marketed by Metrex Research, this product is identified by NDC 55443-0200 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
55443-0200-4
Package Description
3 BOX in 1 CASE / 2 BOTTLE, PLASTIC in 1 BOX (55443-0200-3) / 1000 mL in 1 BOTTLE, PLASTIC (55443-0200-2)
Product Code
55443-0200
11-Digit Billing Format
55443020004

Clinical Specifications

Proprietary Name
Vionexus
Dosage Form
-
Usage Information
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

Regulatory & Marketing

Labeler Name
Metrex Research
FDA Application #
part333E
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
01-01-1992
Listing Expiration
12-31-2017
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage

The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

* Please review the full disclaimer at the bottom of this page.

Other Available Packages

The following commercial packages are registered under the same Product NDC (55443-0200). Click a package code to view its specific billing and regulatory data.

55443-0200-5
48 BOTTLE, PLASTIC in 1 CASE / 59 mL in 1 BOTTLE, PLASTIC (55443-0200-1)

* Please review the full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 55443-0200-4 identifies a specific commercial package of 3 box in 1 case / 2 bottle, plastic in 1 box (55443-0200-3) / 1000 ml in 1 bottle, plastic (55443-0200-2) of Vionexus, labeled by Metrex Research. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Metrex Research on January 01, 1992. The current certification is valid through December 31, 2017.

How is this Metrex Research product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55443020004. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
55443-0200-4
11-Digit CMS (5-4-2)
55443-0200-04

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.