Muscle Cramp Pain Reliever Tablet
NDC Package 43689-0022-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Muscle Cramp Pain Reliever (causticum, colocynthis, cuprum metallicum, magnesia phosphorica, phytolacca decandra, rhus tox, stannum metallicum, veratrum album) tablets is temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, feet, hips and back. This formulation utilizes a tablet delivery system. Marketed by The Magni Company, this product is identified by NDC 43689-0022.

Identification & Billing

NDC Package Code
43689-0022-2
Package Description
1 BOTTLE in 1 CARTON / 125 TABLET in 1 BOTTLE (43689-0022-1)
Product Code
43689-0022
11-Digit Billing Format
43689002202

Clinical Specifications

Proprietary Name
Muscle Cramp Pain Reliever
Non-Proprietary Name
Causticum, Colocynthis, Cuprum Metallicum, Magnesia Phosphorica, Phytolacca Decandra, Rhus Tox, Stannum Metallicum, Veratrum Album
Substance Name
Causticum; Citrullus Colocynthis Fruit Pulp; Copper; Magnesium Phosphate, Dibasic Trihydrate; Phytolacca Americana Root; Tin; Toxicodendron Pubescens Leaf; Veratrum Album Root
Dosage Form
Tablet - A solid dosage form containing medicinal substances with or without suitable diluents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
Temporarily relieves the symptoms of pain, stiffness and cramping in joints, legs, feet, hips and back.

Regulatory & Marketing

Labeler Name
The Magni Company
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
09-18-2019
Listing Expiration
12-31-2026
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43689-0022-2 identifies a specific commercial package of 1 bottle in 1 carton / 125 tablet in 1 bottle (43689-0022-1) of Muscle Cramp Pain Reliever, a human over the counter drug labeled by The Magni Company. This tablet is formulated for oral use and contains causticum; citrullus colocynthis fruit pulp; copper; magnesium phosphate, dibasic trihydrate; phytolacca americana root; tin; toxicodendron pubescens leaf; veratrum album root as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by The Magni Company on September 18, 2019. The current certification is valid through December 31, 2026.

How is this The Magni Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43689002202. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43689-0022-2
11-Digit CMS (5-4-2)
43689-0022-02

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.