Trauma Plus Gel
NDC Package 44911-0446-1
Package Information
Trauma Plus Gel (calendula officinalis, arnica montana, hypericum perforatum, symphytum officinale, bellis perennis, ledum palustre, sulphuricum acidum, calcarea fluorica, ferrum phosphoricum, rhus tox, ruta graveolens, natrum sulphuricum) gel is for temporary relief of pain associated with bumps, bruises, abrasions, strains, sprains, fractures, stiffness; for all minor injuries.****These statements are based upon traditional homeopathic practice. This formulation utilizes a gel delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0446.
Identification & Billing
Clinical Specifications
- ARNICA MONTANA 1 [hp_X]/g
- BELLIS PERENNIS 12 [hp_X]/g
- CALCIUM FLUORIDE 30 [hp_X]/g
- CALENDULA OFFICINALIS FLOWERING TOP 1 [hp_X]/g
- COMFREY ROOT 6 [hp_X]/g
- FERROSOFERRIC PHOSPHATE 30 [hp_X]/g
- HYPERICUM PERFORATUM 1 [hp_X]/g
- LEDUM PALUSTRE TWIG 12 [hp_X]/g
- RUTA GRAVEOLENS FLOWERING TOP 30 [hp_X]/g
- SODIUM SULFATE 30 [hp_C]/g
- SULFURIC ACID 12 [hp_X]/g
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/g
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0446 - Trauma Plus Gel
- 44911-0446-1 - 57 g in 1 TUBE
- 44911-0446 - Trauma Plus Gel
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 44911-0446-1 identifies a specific commercial package of 57 g in 1 tube of Trauma Plus Gel, a human over the counter drug labeled by Energique, Inc.. This gel is formulated for topical use and contains arnica montana; bellis perennis; calcium fluoride; calendula officinalis flowering top; comfrey root; ferrosoferric phosphate; hypericum perforatum; ledum palustre twig; ruta graveolens flowering top; sodium sulfate; sulfuric acid; 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 February 08, 2018. 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: 44911044601. 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.