V Liquid
NDC Package 44911-0680-1
Package Information
V (anas barbariae, hepatis et cordis extractum, arsenicum album, belladonna, bryonia (alba), carcinosin, echinacea (angustifolia), eupatorium perfoliatum, gelsemium sempervirens, lycopodium clavatum, natrum muriaticum, phosphoricum acidum, phosphorus, pyrogenium, rhus tox, sulphur) liquids is • Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional.• Consult a physician for use in children under 12 years of age. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0680.
Identification & Billing
Clinical Specifications
- ARSENIC TRIOXIDE 30 [hp_X]/mL
- ATROPA BELLADONNA 30 [hp_X]/mL
- BRYONIA ALBA ROOT 30 [hp_X]/mL
- CAIRINA MOSCHATA HEART/LIVER AUTOLYSATE 30 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 30 [hp_X]/mL
- EUPATORIUM PERFOLIATUM FLOWERING TOP 30 [hp_X]/mL
- GELSEMIUM SEMPERVIRENS ROOT 30 [hp_X]/mL
- HUMAN BREAST TUMOR CELL 30 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 30 [hp_X]/mL
- PHOSPHORIC ACID 30 [hp_X]/mL
- PHOSPHORUS 30 [hp_X]/mL
- RANCID BEEF 30 [hp_X]/mL
- SODIUM CHLORIDE 30 [hp_X]/mL
- SULFUR 30 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 30 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0680 - V
- 44911-0680-1 - 60 mL in 1 BOTTLE, DROPPER
- 44911-0680 - V
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 44911-0680-1 identifies a specific commercial package of 60 ml in 1 bottle, dropper of V HP, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arsenic trioxide; atropa belladonna; bryonia alba root; cairina moschata heart/liver autolysate; echinacea angustifolia whole; eupatorium perfoliatum flowering top; gelsemium sempervirens root; human breast tumor cell; lycopodium clavatum spore; phosphoric acid; phosphorus; rancid beef; sodium chloride; sulfur; 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 23, 2023. 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: 44911068001. 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.