Artalgia Liquid
NDC Package 45341-0002-1
Package Information
Artalgia (carduus marianus, arnica montana, agaricus muscarius, baryta carbonica, bellis perennis, glonoinum, hamamelis virginiana, mercurius solubilis, plumbum metallicum, secale cornutum, vanadium metallicum, carbo vegetabilis, hypericum perforatum, phosphorus pulsatilla (pratensis), rhus tox) liquids is for temporary relief of numbness, tingling, discoloration, coldness, and burning of the lower extremities. This formulation utilizes a liquid delivery system. Marketed by Todd Horton Dpm, this product is identified by NDC 45341-0002.
Identification & Billing
Clinical Specifications
- ACTIVATED CHARCOAL 30 [hp_X]/mL
- AMANITA MUSCARIA FRUITING BODY 12 [hp_X]/mL
- ARNICA MONTANA WHOLE 3 [hp_X]/mL
- BARIUM CARBONATE 12 [hp_X]/mL
- BELLIS PERENNIS WHOLE 12 [hp_X]/mL
- CLAVICEPS PURPUREA SCLEROTIUM 12 [hp_X]/mL
- HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK 12 [hp_X]/mL
- HYPERICUM PERFORATUM WHOLE 30 [hp_X]/mL
- LEAD 12 [hp_X]/mL
- MERCURIUS SOLUBILIS 12 [hp_X]/mL
- MILK THISTLE 3 [hp_X]/mL
- NITROGLYCERIN 12 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL
- PULSATILLA PRATENSIS WHOLE 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
- VANADIUM 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 45341 - Todd Horton Dpm
- 45341-0002 - Artalgia
- 45341-0002-1 - 30 mL in 1 BOTTLE, DROPPER
- 45341-0002 - Artalgia
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 45341-0002-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Artalgia, a human over the counter drug labeled by Todd Horton Dpm. This liquid is formulated for oral use and contains activated charcoal; amanita muscaria fruiting body; arnica montana whole; barium carbonate; bellis perennis whole; claviceps purpurea sclerotium; hamamelis virginiana root bark/stem bark; hypericum perforatum whole; lead; mercurius solubilis; milk thistle; nitroglycerin; phosphorus; pulsatilla pratensis whole; toxicodendron pubescens leaf; vanadium 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 Todd Horton Dpm on July 15, 2020. The current certification is valid through December 31, 2026.
How is this Todd Horton Dpm product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 45341000201. 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.