NDC Package 41163-278-03 Light Moisturizing Antibacterial

Benzalkonium Chloride 0.13% Soap Topical - View Billable Units, 11-Digit Format, RxNorm

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:
41163-278-03
Package Description:
1470 mL in 1 BOTTLE, PUMP
Product Code:
Proprietary Name:
Light Moisturizing Antibacterial
Non-Proprietary Name:
Benzalkonium Chloride 0.13%
Substance Name:
Benzalkonium Chloride
Usage Information:
Wet handsapply palmful to handsscrub thoroughlyrinse thoroughly
11-Digit NDC Billing Format:
41163027803
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:
    United Natural Foods, Inc. Dba Unfi
    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):
    Sample Package:
    No
    FDA Application Number:
    part333A
    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:
    11-01-2013
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    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
    41163-278-681656 mL in 1 BOTTLE, PLASTIC
    41163-278-96221 mL in 1 BOTTLE, PUMP

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 41163-278-03?

    The NDC Packaged Code 41163-278-03 is assigned to a package of 1470 ml in 1 bottle, pump of Light Moisturizing Antibacterial, a human over the counter drug labeled by United Natural Foods, Inc. Dba Unfi. The product's dosage form is soap and is administered via topical form.

    Is NDC 41163-278 included in the NDC Directory?

    Yes, Light Moisturizing Antibacterial with product code 41163-278 is active and included in the NDC Directory. The product was first marketed by United Natural Foods, Inc. Dba Unfi on November 01, 2013 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 41163-278-03?

    The 11-digit format is 41163027803. 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
    5-3-241163-278-035-4-241163-0278-03