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  5. NDC Package Code: 43689-0055-1 Magnilife Knee Pain Relief Gel

NDC Package 43689-0055-1 Magnilife Knee Pain Relief Gel

Arnica Montana Flower,Toxicodendron Pubescens Leaf Gel 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:
43689-0055-1
Package Description:
113 g in 1 JAR
Product Code:
43689-0055
Proprietary Name:
Magnilife Knee Pain Relief Gel
Non-Proprietary Name:
Arnica Montana Flower, Toxicodendron Pubescens Leaf
Substance Name:
Arnica Montana Flower; Toxicodendron Pubescens Leaf
Usage Information:
Adults and children 12 years and older, generously apply and massage into affected areas.
11-Digit NDC Billing Format:
43689005501
Product Type:
Human Otc Drug
Labeler Name:
The Magni Company
Dosage Form:
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
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):
  • ARNICA MONTANA FLOWER 1 [hp_X]/g
  • TOXICODENDRON PUBESCENS LEAF 4 [hp_X]/g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    02-10-2022
    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 43689-0055-1?

    The NDC Packaged Code 43689-0055-1 is assigned to a package of 113 g in 1 jar of Magnilife Knee Pain Relief Gel, a human over the counter drug labeled by The Magni Company. The product's dosage form is gel and is administered via topical form.

    Is NDC 43689-0055 included in the NDC Directory?

    Yes, Magnilife Knee Pain Relief Gel with product code 43689-0055 is active and included in the NDC Directory. The product was first marketed by The Magni Company on February 10, 2022 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 43689-0055-1?

    The 11-digit format is 43689005501. 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 5-4-1 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
    5-4-143689-0055-15-4-243689-0055-01