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  5. NDC Package Code: 20276-138-75 Lucky Super Soft Foaming

NDC Package 20276-138-75 Lucky Super Soft Foaming

Benzalkonium Chloride Soap 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:
20276-138-75
Package Description:
222 mL in 1 BOTTLE, PUMP
Product Code:
20276-138
Proprietary Name:
Lucky Super Soft Foaming
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
■ wet hands and apply soap ■ lather all surfaces of hands and fingers by rubbing vigorously for at least 20 seconds ■ rinse hands well and dry
11-Digit NDC Billing Format:
20276013875
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:
    Delta Brands, Inc
    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):
  • BENZALKONIUM CHLORIDE .13 g/100mL
    • 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:
    01-29-2021
    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 20276-138-75?

    The NDC Packaged Code 20276-138-75 is assigned to a package of 222 ml in 1 bottle, pump of Lucky Super Soft Foaming, a human over the counter drug labeled by Delta Brands, Inc. The product's dosage form is soap and is administered via topical form.

    Is NDC 20276-138 included in the NDC Directory?

    Yes, Lucky Super Soft Foaming with product code 20276-138 is active and included in the NDC Directory. The product was first marketed by Delta Brands, Inc on January 29, 2021 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 20276-138-75?

    The 11-digit format is 20276013875. 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
    5-3-220276-138-755-4-220276-0138-75