Fatigue Nosode Eb Liquid
NDC Package 44911-0608-1
Package Information
Fatigue Nosode Eb (astragalus membranaceus, echinacea (angustifolia), phytolacca decandra, hydrastis canadensis, aranea diadema, iridium metallicum, lycopodium clavatum, rhus tox, silicea, sepia, epstein-barr virus nosode) liquids May temporarily relieve fever with indigestion, muscular aches and weakness.****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 44911-0608.
Identification & Billing
Clinical Specifications
- ARANEUS DIADEMATUS 12 [hp_X]/mL
- ASTRAGALUS PROPINQUUS ROOT 3 [hp_X]/mL
- ECHINACEA ANGUSTIFOLIA WHOLE 3 [hp_X]/mL
- GOLDENSEAL 6 [hp_X]/mL
- HUMAN HERPESVIRUS 4 30 [hp_C]/mL
- IRIDIUM 12 [hp_X]/mL
- LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
- PHYTOLACCA AMERICANA ROOT 4 [hp_X]/mL
- SEPIA OFFICINALIS JUICE 12 [hp_X]/mL
- SILICON DIOXIDE 12 [hp_X]/mL
- TOXICODENDRON PUBESCENS LEAF 12 [hp_X]/mL
Regulatory & Marketing
Hierarchy Structure
- 44911 - Energique, Inc.
- 44911-0608 - Fatigue Nosode Eb
- 44911-0608-1 - 30 mL in 1 BOTTLE, DROPPER
- 44911-0608 - Fatigue Nosode Eb
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 44911-0608-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Fatigue Nosode Eb, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains araneus diadematus; astragalus propinquus root; echinacea angustifolia whole; goldenseal; human herpesvirus 4; iridium; lycopodium clavatum spore; phytolacca americana root; sepia officinalis juice; silicon dioxide; 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 May 19, 2021. 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: 44911060801. 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.