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  5. NDC Package Code: 68041-512-01 Foaming Antibacterial Handsoap

NDC Package 68041-512-01 Foaming Antibacterial Handsoap

Benzalkonium Chloride Liquid 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:
68041-512-01
Package Description:
3780 mL in 1 BOTTLE
Product Code:
68041-512
Proprietary Name:
Foaming Antibacterial Handsoap
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Read the entire label before using this product.Ready to use without dilution.Dispense 2 pumps of product onto palm of hand and scrub thoroughly over all surfaces of both hands.Rinse with clean water and dry.
11-Digit NDC Billing Format:
68041051201
Product Type:
Human Otc Drug
Labeler Name:
Chemcor Chemical Corporation
Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
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 .0013 mg/mL
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    07-15-2020
    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.

    Other Product Packages

    The following packages are also available for this product:

    NDC Package CodePackage Description
    68041-512-55207900 mL in 1 DRUM

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 68041-512-01?

    The NDC Packaged Code 68041-512-01 is assigned to a package of 3780 ml in 1 bottle of Foaming Antibacterial Handsoap, a human over the counter drug labeled by Chemcor Chemical Corporation. The product's dosage form is liquid and is administered via topical form.

    Is NDC 68041-512 included in the NDC Directory?

    Yes, Foaming Antibacterial Handsoap with product code 68041-512 is active and included in the NDC Directory. The product was first marketed by Chemcor Chemical Corporation on July 15, 2020 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 68041-512-01?

    The 11-digit format is 68041051201. 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
    5-3-268041-512-015-4-268041-0512-01