Traumeel Ointment
NDC Package 62795-9487-8

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

Package Information

Traumeel (aconitum napellus, arnica montana root, atropa belladonna, bellis perennis, calendula officinalis flowering top, matricaria recutita, echinacea, unspecified, echinacea purpurea, hamamelis virginiana root bark/stem bark, calcium sulfide, hypericum perforatum, mercurius solubilis, achillea millefolium and comfrey root) ointment is directions: Adults and children 4 years and older: Apply generously to affected areas 2 to 3 times daily, or as directedby your health professional. This formulation utilizes a ointment delivery system. Marketed by Medinatura Inc, this product is identified by NDC 62795-9487.

Identification & Billing

NDC Package Code
62795-9487-8
Package Description
1 TUBE in 1 CARTON / 100 g in 1 TUBE
Product Code
62795-9487
11-Digit Billing Format
62795948708
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
100 GM

Clinical Specifications

Proprietary Name
Traumeel
Non-Proprietary Name
Aconitum Napellus, Arnica Montana Root, Atropa Belladonna, Bellis Perennis, Calendula Officinalis Flowering Top, Matricaria Recutita, Echinacea, Unspecified, Echinacea Purpurea, Hamamelis Virginiana Root Bark/stem Bark, Calcium Sulfide, Hypericum Perforatum, Mercurius Solubilis, Achillea Millefolium And Comfrey Root
Substance Name
Achillea Millefolium; Aconitum Napellus; Arnica Montana Root; Atropa Belladonna; Bellis Perennis; Calcium Sulfide; Calendula Officinalis Flowering Top; Comfrey Root; Echinacea Purpurea; Echinacea, Unspecified; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum; Matricaria Recutita; Mercurius Solubilis
Dosage Form
Ointment - A semisolid3 dosage form, usually containing <20% water and volatiles5 and >50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
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)
Usage Information
Directions: Adults and children 4 years and older: Apply generously to affected areas 2 to 3 times daily, or as directedby your health professional. Massage thoroughly into skin. Traumeel® may be applied using mild compression bandagingand/or occlusive bandaging. For children under 4, use as directed by your health professional.

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
12-14-2021
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 62795-9487-8 identifies a specific commercial package of 1 tube in 1 carton / 100 g in 1 tube of Traumeel, a human over the counter drug labeled by Medinatura Inc. This product is billed per "GM" gram and contains an estimated amount of 100 billable units per package. This ointment is formulated for topical use and contains achillea millefolium; aconitum napellus; arnica montana root; atropa belladonna; bellis perennis; calcium sulfide; calendula officinalis flowering top; comfrey root; echinacea purpurea; echinacea, unspecified; hamamelis virginiana root bark/stem bark; hypericum perforatum; matricaria recutita; mercurius solubilis 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 December 14, 2021. 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: 62795948708. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 100 total billable units per package. 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)
62795-9487-8
11-Digit CMS (5-4-2)
62795-9487-08

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