1. Home
  2. Labeler Index
  3. Unico International Trading Corporation
  4. 74680-201
  5. NDC Package Code: 74680-201-86 Wipex

NDC Package 74680-201-86 Wipex

Antibacterial Wipe Cloth Topical - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. 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:
74680-201-86
Package Description:
800 mg in 1 PACKAGE
Product Code:
74680-201
Proprietary Name:
Wipex
Non-Proprietary Name:
Antibacterial Wipe
Substance Name:
Benzalkonium Chloride
Usage Information:
This product is used as Antibacterial
11-Digit NDC Billing Format:
74680020186
NDC to RxNorm Crosswalk:
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 % Topical Swab
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Pad
  • RxCUI: 1038558 - benzalkonium chloride 0.13 GM per 100 GM Topical Swab
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Unico International Trading Corporation
    Dosage Form:
    Cloth - A large piece of relatively flat, absorbent material that contains a drug. It is typically used for applying medication or for cleansing.
    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):
  • BENZALKONIUM CHLORIDE .13 mg/mg
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-22-2024
    Listing Expiration Date:
    12-31-2025
    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.

    Frequently Asked Questions

    What is NDC 74680-201-86?

    The NDC Packaged Code 74680-201-86 is assigned to a package of 800 mg in 1 package of Wipex, a human over the counter drug labeled by Unico International Trading Corporation. The product's dosage form is cloth and is administered via topical form.

    Is NDC 74680-201 included in the NDC Directory?

    Yes, Wipex with product code 74680-201 is active and included in the NDC Directory. The product was first marketed by Unico International Trading Corporation on March 22, 2024 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 74680-201-86?

    The 11-digit format is 74680020186. 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 5-3-2 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
    5-3-274680-201-865-4-274680-0201-86