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  5. NDC Package Code: 54622-313-01 Gp Pbu Antimicrobial Foam

NDC Package 54622-313-01 Gp Pbu Antimicrobial Foam

Benzalkonium Chloride Solution 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:
54622-313-01
Package Description:
1200 mL in 1 BOTTLE, DISPENSING
Product Code:
54622-313
Proprietary Name:
Gp Pbu Antimicrobial Foam
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Wet hands, apply soap, rub hands togetehr vigorously for at least 20 seconds.Rinse and dry hands thoroughly.
11-Digit NDC Billing Format:
54622031301
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:
    Georgia Pacific Consumer Products
    Dosage Form:
    Solution - A clear, homogeneous liquid1 dosage form that contains one or more chemical substances dissolved in a solvent or mixture of mutually miscible solvents.
    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 g/100mL
    • Sample Package:
    Yes
    FDA Application Number:
    part333E
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    08-05-2021
    Listing Expiration Date:
    12-31-2024
    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.

    Frequently Asked Questions

    What is NDC 54622-313-01?

    The NDC Packaged Code 54622-313-01 is assigned to a package of 1200 ml in 1 bottle, dispensing of Gp Pbu Antimicrobial Foam, a human over the counter drug labeled by Georgia Pacific Consumer Products. The product's dosage form is solution and is administered via topical form.

    Is NDC 54622-313 included in the NDC Directory?

    Yes, Gp Pbu Antimicrobial Foam with product code 54622-313 is active and included in the NDC Directory. The product was first marketed by Georgia Pacific Consumer Products on August 05, 2021 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 54622-313-01?

    The 11-digit format is 54622031301. 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
    5-3-254622-313-015-4-254622-0313-01