NDC 55443-0600 Vionexus

Chloroxylenol

NDC Product Code 55443-0600

NDC 55443-0600-3

Package Description: 3 BOX in 1 CASE > 2 BOTTLE, DISPENSING in 1 BOX (55443-0600-2) > 1000 mL in 1 BOTTLE, DISPENSING (55443-0600-1)

NDC Product Information

Vionexus with NDC 55443-0600 is a a human over the counter drug product labeled by Metrex Research. The generic name of Vionexus is chloroxylenol. The product's dosage form is liquid and is administered via topical form.

Labeler Name: Metrex Research

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.

Product Type: Human Otc Drug What kind of product is this?
Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.

Vionexus Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • CHLOROXYLENOL 1 g/100mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • EDETATE SODIUM (UNII: MP1J8420LU)
  • D&C GREEN NO. 8 (UNII: I2W85YOX9L)
  • D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)
  • POTASSIUM COCOATE (UNII: F8U72V8ZXP)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.

Product Labeler Information

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

Labeler Name: Metrex Research
Labeler Code: 55443
FDA Application Number: part333A What is the FDA Application Number?
This corresponds to the NDA, ANDA, or BLA number reported by the labeler for products which have the corresponding Marketing Category designated. If the designated Marketing Category is OTC Monograph Final or OTC Monograph Not Final, then the Application number will be the CFR citation corresponding to the appropriate Monograph (e.g. “part 341”). For unapproved drugs, this field will be null.

Marketing Category: OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final. What is the Marketing Category?
Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Start Marketing Date: 10-01-2019 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Vionexus Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Drug Facts

Active Ingredients Purpose
Chloroxylenol 1.0%................Healthcare personnel handwash

Uses

  • Handwash to help reduce bacteria that potentially can cause diseasehelps prevent cross contamination by hand contactrecommended for repeated use

Warnings

For external use only

Keep Out Of Reach Of Children

In case of accidental ingestion, seek medical attention or contact a poison control center immediately.

Directions

  • Wet hands and forearmsapply 5-10 ml to hands and forearmsscrub thoroughly for at least 30 seconds and include fingertips and cuticlesrinse

Inactive Ingredients

D&C Green 5, D&C Green 8, fragrance, potassium cocoate, purified water, tetrasodium EDTA

Indications & Usage

Healthcare Personnel Handwash

* Please review the disclaimer below.