Injury-rescue Liquid
NDC Package 55714-4795-1
Package Information
Injury-rescue (aconitum nap, arnica, bellis, calendula, echinacea, gelsemium, hamamelis, hypericum, ledum, phosphorus, rhus toxicodendron, ruta, staphysag., symphytum, hydrastis canadensis.) liquids is formulated for symptoms associated with trauma or medical procedures such as pain, emotional upset, bruising and inflammation. This formulation utilizes a liquid delivery system. Marketed by Newton Laboratories, Inc., this product is identified by NDC 55714-4795.
Identification & Billing
Clinical Specifications
- ACONITUM NAPELLUS 20 [hp_X]/mL
- ARNICA MONTANA 20 [hp_X]/mL
- BELLIS PERENNIS 20 [hp_X]/mL
- CALENDULA OFFICINALIS FLOWERING TOP 20 [hp_X]/mL
- COMFREY ROOT 20 [hp_X]/mL
- DELPHINIUM STAPHISAGRIA SEED 20 [hp_X]/mL
- ECHINACEA, UNSPECIFIED 20 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT 20 [hp_X]/mL
- GOLDENSEAL 11 [hp_X]/mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 20 [hp_X]/mL
- HYPERICUM PERFORATUM 20 [hp_X]/mL
- PHOSPHORUS 20 [hp_X]/mL
- RHODODENDRON TOMENTOSUM LEAFY TWIG 20 [hp_X]/mL
- RUTA GRAVEOLENS FLOWERING TOP 20 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 20 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 55714 - Newton Laboratories, Inc.
- 55714-4795 - Injury-rescue
- 55714-4795-1 - 30 mL in 1 BOTTLE, GLASS
- 55714-4795 - Injury-rescue
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 55714-4795-1 identifies a specific commercial package of 30 ml in 1 bottle, glass of Injury-rescue, a human over the counter drug labeled by Newton Laboratories, Inc.. This liquid is formulated for oral use and contains aconitum napellus; arnica montana; bellis perennis; calendula officinalis flowering top; comfrey root; delphinium staphisagria seed; echinacea, unspecified; gelsemium sempervirens root; goldenseal; hamamelis virginiana root bark/stem bark; hypericum perforatum; phosphorus; rhododendron tomentosum leafy twig; ruta graveolens flowering top; 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 Newton Laboratories, Inc. on September 02, 2019. The current certification is valid through December 31, 2026.
How is this Newton Laboratories, Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 55714479501. 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.