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  5. NDC Package Code: 47593-404-41 Digisan E

NDC Package 47593-404-41 Digisan E

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:
47593-404-41
Package Description:
750 mL in 1 BOTTLE, PLASTIC
Product Code:
47593-404
Proprietary Name:
Digisan E
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Wet hands and remove soildispense palmfulspread to cover hands, rub in wellair dry, do not rinse or towel dry
11-Digit NDC Billing Format:
47593040441
NDC to RxNorm Crosswalk:
  • RxCUI: 1038799 - benzalkonium chloride 0.1 % Topical Foam
  • RxCUI: 1038799 - benzalkonium chloride 1 MG/ML Topical Foam
  • RxCUI: 1038834 - DigiSan E Foam 0.1 % Topical Foam
  • RxCUI: 1038834 - benzalkonium chloride 1 MG/ML Topical Foam [DigiSan E Foam]
  • RxCUI: 1038834 - DigiSan E Foam 1 MG/ML Topical Foam
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ecolab Inc.
    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 1 mg/mL
    • Sample Package:
    No
    FDA Application Number:
    505G(a)(3)
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    11-04-2003
    Listing Expiration Date:
    12-31-2025
    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 47593-404-41?

    The NDC Packaged Code 47593-404-41 is assigned to a package of 750 ml in 1 bottle, plastic of Digisan E, a human over the counter drug labeled by Ecolab Inc.. The product's dosage form is solution and is administered via topical form.

    Is NDC 47593-404 included in the NDC Directory?

    Yes, Digisan E with product code 47593-404 is active and included in the NDC Directory. The product was first marketed by Ecolab Inc. on November 04, 2003 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 47593-404-41?

    The 11-digit format is 47593040441. 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
    5-3-247593-404-415-4-247593-0404-41