NDC Package 73788-108-01 Cleanhands

Benzalkonium Chloride 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:
73788-108-01
Package Description:
20 BOTTLE in 1 CARTON / 500 g in 1 BOTTLE
Product Code:
Proprietary Name:
Cleanhands
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
●Pump into hands, wet as needed. ●Lather vigorously for at least 15 seconds. ●Wash skin, rinse thoroughly and dry.
11-Digit NDC Billing Format:
73788010801
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:
    Hangzhou Huiji Biotechnology Co., Ltd.
    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:
    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:
    08-25-2020
    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.

    Frequently Asked Questions

    What is NDC 73788-108-01?

    The NDC Packaged Code 73788-108-01 is assigned to a package of 20 bottle in 1 carton / 500 g in 1 bottle of Cleanhands, a human over the counter drug labeled by Hangzhou Huiji Biotechnology Co., Ltd.. The product's dosage form is soap and is administered via topical form.

    Is NDC 73788-108 included in the NDC Directory?

    Yes, Cleanhands with product code 73788-108 is active and included in the NDC Directory. The product was first marketed by Hangzhou Huiji Biotechnology Co., Ltd. on August 25, 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 73788-108-01?

    The 11-digit format is 73788010801. 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
    5-3-273788-108-015-4-273788-0108-01