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  5. NDC Package Code: 50241-259-02 Mg Dermasan

NDC Package 50241-259-02 Mg Dermasan

N/a 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:
50241-259-02
Package Description:
1 BOTTLE, PLASTIC in 1 BOX / 3756 g in 1 BOTTLE, PLASTIC (50241-259-01)
Product Code:
50241-259
Proprietary Name:
Mg Dermasan
Non-Proprietary Name:
N/a
Substance Name:
Benzalkonium Chloride
Usage Information:
Pump a small amount of foam into palm of hand.Rub thoroughly over all surfaces of both hands.Rub hands together briskly until dry.
11-Digit NDC Billing Format:
50241025902
NDC to RxNorm Crosswalk:
  • RxCUI: 1038791 - benzalkonium chloride 0.1 % Topical Solution
  • RxCUI: 1038791 - benzalkonium chloride 1 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Morgan Gallacher 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 g/100g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    10-01-2018
    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 50241-259-02?

    The NDC Packaged Code 50241-259-02 is assigned to a package of 1 bottle, plastic in 1 box / 3756 g in 1 bottle, plastic (50241-259-01) of Mg Dermasan, a human over the counter drug labeled by Morgan Gallacher Inc.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 50241-259 included in the NDC Directory?

    Yes, Mg Dermasan with product code 50241-259 is active and included in the NDC Directory. The product was first marketed by Morgan Gallacher Inc. on October 01, 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 50241-259-02?

    The 11-digit format is 50241025902. 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
    5-3-250241-259-025-4-250241-0259-02