Traumatone Liquid
NDC Package 44911-0714-1
Package Information
Traumatone (calendula officinalis, symphytum officinale, arnica montana, bellis perennis, camphora, hamamelis virginiana, hypericum perforatum, ledum palustre, natrum sulphuricum, phosphorus, rhus tox, ruta graveolens, staphysagria, strontium carbonicum) liquids is adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0714.
Identification & Billing
Clinical Specifications
- ARNICA MONTANA WHOLE 12 [hp_X]/mL
- BELLIS PERENNIS WHOLE 12 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 3 [hp_X]/mL
- CAMPHOR (NATURAL) 12 [hp_X]/mL
- COMFREY ROOT 6 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 12 [hp_X]/mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 12 [hp_X]/mL
- HYPERICUM PERFORATUM WHOLE 12 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 12 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 12 [hp_X]/mL
- SODIUM SULFATE 12 [hp_X]/mL
- STRONTIUM CARBONATE 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0714 - Traumatone
- 44911-0714-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0714 - Traumatone
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 44911-0714-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Traumatone, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arnica montana whole; bellis perennis whole; calendula officinalis flowering top; camphor (natural); comfrey root; delphinium staphisagria seed; hamamelis virginiana root bark/stem bark; hypericum perforatum whole; phosphorus; rhododendron tomentosum leafy twig; ruta graveolens flowering top; sodium sulfate; strontium carbonate; toxicodendron pubescens leaf 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 Energique, Inc. on August 01, 2024. The current certification is valid through December 31, 2026.
How is this Energique, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911071401. 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:
Note: The zero is added to the Package segment to maintain the 5-4-2 structure.