Free Radistat Liquid
NDC Package 44911-0464-1
Package Information
Free Radistat (baptisia tinctoria, echinacea (angustifolia), fucus vesiculosus, uva-ursi, phytolacca decandra, arsenicum album, aurum metallicum, ferrum phosphoricum, iodium, iridium metallicum, lachesis mutus, zincum metallicum, cadmium sulphuratum) liquids May temporarily relieve weakness, tiredness, and general exhaustion.****Claims based on traditional homeopathic practice, not accepted medical evidence. This formulation utilizes a liquid delivery system. Marketed by Energique, Inc., this product is identified by NDC 44911-0464.
Identification & Billing
Clinical Specifications
- ARCTOSTAPHYLOS UVA-URSI LEAF 3 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL
- BAPTISIA TINCTORIA ROOT 3 [hp_X]/mL
- CADMIUM SULFIDE 13 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- FERROSOFERRIC PHOSPHATE 12 [hp_X]/mL
- FUCUS VESICULOSUS 3 [hp_X]/mL
- GOLD 12 [hp_X]/mL
- IODINE 12 [hp_X]/mL
- IRIDIUM 12 [hp_X]/mL
- LACHESIS MUTA VENOM 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- ZINC 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0464 - Free Radistat
- 44911-0464-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0464 - Free Radistat
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 44911-0464-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Free Radistat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains arctostaphylos uva-ursi leaf; arsenic trioxide; baptisia tinctoria root; cadmium sulfide; echinacea angustifolia whole; ferrosoferric phosphate; fucus vesiculosus; gold; iodine; iridium; lachesis muta venom; phytolacca americana root; zinc 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 17, 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: 44911046401. 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.