Traumex Tablet, Chewable
NDC Package 62795-2302-2

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

Package Information

Traumex (arnica montana whole, calendula officinalis flowering top, hamamelis virginiana root bark/stem bark, baptisia tinctoria root, bellis perennis whole, echinacea angustifolia whole, aconitum napellus whole, matricaria chamomilla whole, achillea millefolium whole, atropa belladonna, hypericum perforatum whole, ruta graveolens flowering top and comfrey root) tablets is  At first sign of symptoms: Adults and children 4 yearsand older: 1 tablet every 1/2 to 1 hour until symptoms lessen, thencontinue with standard dosage. This formulation utilizes a tablet, chewable delivery system. Marketed by Medinatura Inc, this product is identified by NDC 62795-2302.

Identification & Billing

NDC Package Code
62795-2302-2
Package Description
60 TABLET, CHEWABLE in 1 BOTTLE
Product Code
62795-2302
11-Digit Billing Format
62795230202

Clinical Specifications

Proprietary Name
Traumex
Non-Proprietary Name
Arnica Montana Whole, Calendula Officinalis Flowering Top, Hamamelis Virginiana Root Bark/stem Bark, Baptisia Tinctoria Root, Bellis Perennis Whole, Echinacea Angustifolia Whole, Aconitum Napellus Whole, Matricaria Chamomilla Whole, Achillea Millefolium Whole, Atropa Belladonna, Hypericum Perforatum Whole, Ruta Graveolens Flowering Top And Comfrey Root
Substance Name
Achillea Millefolium Whole; Aconitum Napellus Whole; Arnica Montana Whole; Atropa Belladonna; Baptisia Tinctoria Root; Bellis Perennis Whole; Calendula Officinalis Flowering Top; Comfrey Root; Echinacea Angustifolia Whole; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum Whole; Matricaria Chamomilla Whole; Ruta Graveolens Flowering Top
Dosage Form
Tablet, Chewable - A solid dosage form containing medicinal substances with or without suitable diluents that is intended to be chewed, producing a pleasant tasting residue in the oral cavity that is easily swallowed and does not leave a bitter or unpleasant after-taste.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
 At first sign of symptoms: Adults and children 4 yearsand older: 1 tablet every 1/2 to 1 hour until symptoms lessen, thencontinue with standard dosage. Standard dosage: Adults andchildren 4 years and older: 3 tablets per day, taking 1 tablet every4-6 hours. Do not exceed 12 tablets in 24 hours. For childrenunder 4 years, consult your health professional. Allow tablets todissolve completely in the mouth, do not swallow

Regulatory & Marketing

Labeler Name
Medinatura Inc
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
03-20-2023
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 62795-2302-2 identifies a specific commercial package of 60 tablet, chewable in 1 bottle of Traumex, a human over the counter drug labeled by Medinatura Inc. This tablet, chewable is formulated for oral use and contains achillea millefolium whole; aconitum napellus whole; arnica montana whole; atropa belladonna; baptisia tinctoria root; bellis perennis whole; calendula officinalis flowering top; comfrey root; echinacea angustifolia whole; hamamelis virginiana root bark/stem bark; hypericum perforatum whole; matricaria chamomilla whole; ruta graveolens flowering top 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 Medinatura Inc on March 20, 2023. The current certification is valid through December 31, 2026.

How is this Medinatura Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62795230202. 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)
62795-2302-2
11-Digit CMS (5-4-2)
62795-2302-02

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