Arteriotone Liquid
NDC Package 44911-0230-1
Package Information
Arteriotone (baptisia tinctoria, cactus grandiflorus, echinacea (angustifolia), adonis vernalis, agnus castus, arnica montana, aurum metallicum, digitalis purpurea, glonoinum, vanadium metallicum) liquids is for temporary relief of swollen extremities, feel bruised, cold clammy feet, mild burning pains in lower limbs, leg cramps.****These statements are based upon traditional homeopathic practice. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0230.
Identification & Billing
Clinical Specifications
- ADONIS VERNALIS WHOLE 12 [hp_X]/mL
- ARNICA MONTANA WHOLE 12 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- CHASTE TREE FRUIT 12 [hp_X]/mL
- DIGITALIS 12 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- GOLD 12 [hp_X]/mL
- NITROGLYCERIN 12 [hp_X]/mL
- SELENICEREUS GRANDIFLORUS STEM 3 [hp_X]/mL
- VANADIUM 12 [hp_X]/mL
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Increased Histamine Release - [PE] (Physiologic Effect)
- Nitrate Vasodilator - [EPC] (Established Pharmacologic Class)
- Nitrates - [CS]
- Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
- Vasodilation - [PE] (Physiologic Effect)
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0230 - Arteriotone
- 44911-0230-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0230 - Arteriotone
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 44911-0230-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Arteriotone, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains adonis vernalis whole; arnica montana whole; baptisia tinctoria root; chaste tree fruit; digitalis; echinacea angustifolia whole; gold; nitroglycerin; selenicereus grandiflorus stem; 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 Energique, Inc. on July 27, 2015. 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: 44911023001. 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.