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  5. NDC Package Code: 65055-201-01 Mertodol Solution

NDC Package 65055-201-01 Mertodol Solution

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:
65055-201-01
Package Description:
25 mL in 1 BOTTLE, PLASTIC
Product Code:
65055-201
Proprietary Name:
Mertodol Solution
Non-Proprietary Name:
Benzalkonium Chloride
Substance Name:
Benzalkonium Chloride
Usage Information:
-Clean the affected area-Apply a small amount of this product on the area 1 to 3 times daily- May be covered with a sterile bandage
11-Digit NDC Billing Format:
65055020101
NDC to RxNorm Crosswalk:
  • RxCUI: 1049254 - benzalkonium chloride 0.13 % Topical Solution
  • RxCUI: 1049254 - benzalkonium chloride 1.3 MG/ML Topical Solution
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Laboratorios Jaloma, S.a. De C.v.
    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 .13 g/100mL
    • Sample Package:
    No
    FDA Application Number:
    M003
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    08-24-2016
    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 65055-201-01?

    The NDC Packaged Code 65055-201-01 is assigned to a package of 25 ml in 1 bottle, plastic of Mertodol Solution, a human over the counter drug labeled by Laboratorios Jaloma, S.a. De C.v.. The product's dosage form is liquid and is administered via topical form.

    Is NDC 65055-201 included in the NDC Directory?

    Yes, Mertodol Solution with product code 65055-201 is active and included in the NDC Directory. The product was first marketed by Laboratorios Jaloma, S.a. De C.v. on August 24, 2016 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 65055-201-01?

    The 11-digit format is 65055020101. 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
    5-3-265055-201-015-4-265055-0201-01