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  5. NDC Package Code: 80989-111-01 Woa Protect

NDC Package 80989-111-01 Woa Protect

View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

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

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:
80989-111-01
Package Description:
20 PACKAGE in 1 CARTON / 4.3 mL in 1 PACKAGE
Product Code:
80989-111
Proprietary Name:
Woa Protect
Usage Information:
Push the capsule's paper seal label as marked on itAllow the tissue paper inside to be completely soaked in the liquidRemove the tissue and thoroughly wipe your hands / objects within TWO minutes after opening otherwise it could dry up.Wait for the hands to dry completelyApply to face, hands, body and object surfaces only. Not suitable for conductive parts
11-Digit NDC Billing Format:
80989011101
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
    • Labeler Name:
    The Woa Consulting Group Ltd
    Sample Package:
    No
    Start Marketing Date:
    11-26-2020
    Listing Expiration Date:
    12-31-2021
    Exclude Flag:
    I
    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 80989-111-01?

    The NDC Packaged Code 80989-111-01 is assigned to a package of 20 package in 1 carton / 4.3 ml in 1 package of Woa Protect, labeled by The Woa Consulting Group Ltd. The product's dosage form is and is administered via form.

    Is NDC 80989-111 included in the NDC Directory?

    No, Woa Protect with product code 80989-111 is excluded from the NDC Directory because it's listing has been INACTIVATED by FDA. The product was first marketed by The Woa Consulting Group Ltd on November 26, 2020 and its listing in the NDC Directory is set to expire on December 31, 2021 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 80989-111-01?

    The 11-digit format is 80989011101. 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
    5-3-280989-111-015-4-280989-0111-01