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  5. NDC Package Code: 81277-179-41 Zest Aqua Antibacterial Hand Zest

NDC Package 81277-179-41 Zest Aqua Antibacterial Hand Zest

Benzalkonium Chloride Soap 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:
81277-179-41
Package Description:
221 mL in 1 BOTTLE, PUMP
Product Code:
81277-179
Proprietary Name:
Zest Aqua Antibacterial Hand Zest
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Uses for handwashing to decrease bacteria on the skin
11-Digit NDC Billing Format:
81277017941
NDC to RxNorm Crosswalk:
  • RxCUI: 1046593 - benzalkonium chloride 0.13 % Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.3 MG/ML Medicated Liquid Soap
  • RxCUI: 1046593 - benzalkonium chloride 1.33 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Tcp Hrb Holdings
    Dosage Form:
    Soap - Any compound of one or more fatty acids, or their equivalents, with an alkali; soap is detergent and is much employed in liniments, enemas, and in making pills. It is also a mild aperient, antacid and antiseptic.
    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/10mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-17-2020
    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 81277-179-41?

    The NDC Packaged Code 81277-179-41 is assigned to a package of 221 ml in 1 bottle, pump of Zest Aqua Antibacterial Hand Zest, a human over the counter drug labeled by Tcp Hrb Holdings. The product's dosage form is soap and is administered via topical form.

    Is NDC 81277-179 included in the NDC Directory?

    Yes, Zest Aqua Antibacterial Hand Zest with product code 81277-179 is active and included in the NDC Directory. The product was first marketed by Tcp Hrb Holdings on June 17, 2020 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 81277-179-41?

    The 11-digit format is 81277017941. 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
    5-3-281277-179-415-4-281277-0179-41