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  5. NDC Package Code: 78890-001-01 Non-alcohol Foaming Hand Wash

NDC Package 78890-001-01 Non-alcohol Foaming Hand Wash

Benzalkonium Chloride 0.10% 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:
78890-001-01
Package Description:
3785 mL in 1 JUG
Product Code:
78890-001
Proprietary Name:
Non-alcohol Foaming Hand Wash
Non-Proprietary Name:
Benzalkonium Chloride 0.10%
Substance Name:
Benzalkonium Chloride
Usage Information:
USE for waterless cleansing of hands to decrease soil on the skin
11-Digit NDC Billing Format:
78890000101
NDC to RxNorm Crosswalk:
  • RxCUI: 1038799 - benzalkonium chloride 0.1 % Topical Foam
  • RxCUI: 1038799 - benzalkonium chloride 1 MG/ML Topical Foam
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Arkansas Correctional Industries
    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 .1 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    06-22-2020
    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
    78890-001-02208198 mL in 1 DRUM

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 78890-001-01?

    The NDC Packaged Code 78890-001-01 is assigned to a package of 3785 ml in 1 jug of Non-alcohol Foaming Hand Wash, a human over the counter drug labeled by Arkansas Correctional Industries. The product's dosage form is liquid and is administered via topical form.

    Is NDC 78890-001 included in the NDC Directory?

    Yes, Non-alcohol Foaming Hand Wash with product code 78890-001 is active and included in the NDC Directory. The product was first marketed by Arkansas Correctional Industries on June 22, 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 78890-001-01?

    The 11-digit format is 78890000101. 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
    5-3-278890-001-015-4-278890-0001-01