1. Home
  2. Labeler Index
  3. Ecolab Inc.
  4. 47593-592
  5. NDC Package Code: 47593-592-41 Swisher

NDC Package 47593-592-41 Swisher

Benzalkonium Chloride Liquid 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:
47593-592-41
Package Description:
750 mL in 1 BOTTLE, PLASTIC
Product Code:
47593-592
Proprietary Name:
Swisher
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
Wash hands to remove soildispense palmfulspread to cover hands, rub in wellair dry, do not rinse or towel dry
11-Digit NDC Billing Format:
47593059241
NDC to RxNorm Crosswalk:
  • RxCUI: 1233282 - benzalkonium chloride 0.1 % Medicated Liquid Soap
  • RxCUI: 1233282 - benzalkonium chloride 1 MG/ML Medicated Liquid Soap
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Ecolab Inc.
    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 mg/mL
    • 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:
    06-15-2018
    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 47593-592-41?

    The NDC Packaged Code 47593-592-41 is assigned to a package of 750 ml in 1 bottle, plastic of Swisher, a human over the counter drug labeled by Ecolab Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 47593-592 included in the NDC Directory?

    Yes, Swisher with product code 47593-592 is active and included in the NDC Directory. The product was first marketed by Ecolab Inc. on June 15, 2018 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 47593-592-41?

    The 11-digit format is 47593059241. 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
    5-3-247593-592-415-4-247593-0592-41