Vionexus Liquid
NDC Package 55443-0400-4

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

Vionexus (alcohol) liquids is wet hands thoroughly with spray, covering entire surface of hands, including finger tips and cuticlesrub vigorously into skin until dryno rinsing or wiping is required. This formulation utilizes a liquid delivery system. Marketed by Metrex Research, Llc, this product is identified by NDC 55443-0400 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
55443-0400-4
Package Description
3 BOX in 1 CASE / 2 BOTTLE, DISPENSING in 1 BOX (55443-0400-3) / 1000 mL in 1 BOTTLE, DISPENSING (55443-0400-2)
Product Code
55443-0400
11-Digit Billing Format
55443040004
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Vionexus
Non-Proprietary Name
Alcohol
Substance Name
Alcohol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
ALCOHOL 72 mL/100mL
Usage Information
Wet hands thoroughly with spray, covering entire surface of hands, including finger tips and cuticlesrub vigorously into skin until dryno rinsing or wiping is required

Regulatory & Marketing

Labeler Name
Metrex Research, Llc
Product Type
Human Otc Drug
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
11-01-2018
Listing Expiration
12-31-2027
Exclude Flag
N
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 (55443-0400). Click a package code to view its specific billing and regulatory data.

55443-0400-5
48 BOTTLE, SPRAY in 1 CASE / 59 mL in 1 BOTTLE, SPRAY (55443-0400-1)
55443-0400-7
12 BOTTLE, SPRAY in 1 CASE / 237 mL in 1 BOTTLE, SPRAY (55443-0400-6)

* 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 55443-0400-4 identifies a specific commercial package of 3 box in 1 case / 2 bottle, dispensing in 1 box (55443-0400-3) / 1000 ml in 1 bottle, dispensing (55443-0400-2) of Vionexus, a human over the counter drug labeled by Metrex Research, Llc. This liquid is formulated for topical use and contains alcohol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Metrex Research, Llc on November 01, 2018. The current certification is valid through December 31, 2027.

How is this Metrex Research, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 55443040004. 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)
55443-0400-4
11-Digit CMS (5-4-2)
55443-0400-04

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