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  5. NDC Package Code: 55443-0085-6 Vionex

NDC Package 55443-0085-6 Vionex

Chloroxylenol Gel Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Other Packages
    3. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
55443-0085-6
Package Description:
24 BOTTLE, PLASTIC in 1 BOX / 118.3 mL in 1 BOTTLE, PLASTIC (55443-0085-5)
Product Code:
55443-0085
Proprietary Name:
Vionex
Non-Proprietary Name:
Chloroxylenol
Substance Name:
Chloroxylenol
Usage Information:
Wet hands and forearmsapply 5 mL or palmful of soap to hands and forearmsscrub thoroughly for 30 secondsrinse and repeat
11-Digit NDC Billing Format:
55443008506
NDC to RxNorm Crosswalk:
  • RxCUI: 1053227 - chloroxylenol 0.52 % Medicated Liquid Soap
  • RxCUI: 1053227 - chloroxylenol 5.2 MG/ML Medicated Liquid Soap
  • RxCUI: 1053230 - VioNex 0.52 % Medicated Liquid Soap
  • RxCUI: 1053230 - chloroxylenol 5.2 MG/ML Medicated Liquid Soap [VioNex]
  • RxCUI: 1053230 - VioNex 5.2 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Metrex Research, Llc
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    Administration Route(s):
  • 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):
  • CHLOROXYLENOL .52 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    01-01-1992
    End Marketing Date:
    10-01-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    55443-0085-112 BOTTLE, PLASTIC in 1 BOX / 532.3 mL in 1 BOTTLE, PLASTIC (55443-0085-2)
    55443-0085-44 BOTTLE, PLASTIC in 1 BOX / 3785.4 mL in 1 BOTTLE, PLASTIC (55443-0085-3)

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 55443-0085-6?

    The NDC Packaged Code 55443-0085-6 is assigned to a package of 24 bottle, plastic in 1 box / 118.3 ml in 1 bottle, plastic (55443-0085-5) of Vionex, a human over the counter drug labeled by Metrex Research, Llc. The product's dosage form is gel and is administered via topical form.

    Is NDC 55443-0085 included in the NDC Directory?

    Yes, Vionex with product code 55443-0085 is active and included in the NDC Directory. The product was first marketed by Metrex Research, Llc on January 01, 1992.

    What is the 11-digit format for NDC 55443-0085-6?

    The 11-digit format is 55443008506. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-155443-0085-65-4-255443-0085-06