NDC Package 20276-431-40 Wet Wipes

Benzalkonium Chloride Swab 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:
20276-431-40
Package Description:
40 SWAB in 1 PACKAGE
Product Code:
Proprietary Name:
Wet Wipes
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
 • for adults and children 2 years and over use on hands and face to clean and refresh, allow skin to air dry.  For children under 2 years of age ask a doctor before use.
11-Digit NDC Billing Format:
20276043140
NDC to RxNorm Crosswalk:
  • RxCUI: 1038856 - benzalkonium Cl 0.1 % Medicated Pad
  • RxCUI: 1038856 - benzalkonium chloride 1 MG/ML Medicated Pad
  • RxCUI: 1038856 - benzalkonium chloride 0.1 % Medicated Wipes
  • RxCUI: 1038856 - benzalkonium chloride 0.1 % Topical Swab
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Delta Brands, Inc
    Dosage Form:
    Swab - A small piece of relatively flat absorbent material that contains a drug. A swab may also be attached to one end of a small stick. A swab is typically used for applying medication or for cleansing.
    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:
    01-23-2007
    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
    20276-431-1616 SWAB in 1 PACKAGE
    20276-431-3030 SWAB in 1 PACKAGE
    20276-431-3636 SWAB in 1 PACKAGE
    20276-431-5050 SWAB in 1 PACKAGE
    20276-431-6060 SWAB in 1 PACKAGE
    20276-431-8080 SWAB in 1 PACKAGE

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 20276-431-40?

    The NDC Packaged Code 20276-431-40 is assigned to a package of 40 swab in 1 package of Wet Wipes, a human over the counter drug labeled by Delta Brands, Inc. The product's dosage form is swab and is administered via topical form.

    Is NDC 20276-431 included in the NDC Directory?

    Yes, Wet Wipes with product code 20276-431 is active and included in the NDC Directory. The product was first marketed by Delta Brands, Inc on January 23, 2007 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 20276-431-40?

    The 11-digit format is 20276043140. 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
    5-3-220276-431-405-4-220276-0431-40