Lymphastat Liquid
NDC Package 44911-0615-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Lymphastat (baptisia tinctoria, echinacea (angustifolia), lobelia inflata, lomatium dissectum, hydrastis canadensis, lung (suis), phytolacca decandra, symphytum officinale, aconitum napellus, arsenicum album, belladonna, bryonia (alba), causticum, eupatorium perfoliatum, ferrum phosphoricum, gelsemium sempervirens, hypericum perforatum, kali carbonicum, lachesis mutus, natrum sulphuricum, phosphorus, pulsatilla (pratensis), rhus tox, silicea, sulphur, pyrogenium) liquids May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.****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 44911-0615.

Identification & Billing

NDC Package Code
44911-0615-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
44911-0615
11-Digit Billing Format
44911061501

Clinical Specifications

Proprietary Name
Lymphastat
Non-Proprietary Name
Baptisia Tinctoria, Echinacea (angustifolia), Lobelia Inflata, Lomatium Dissectum, Hydrastis Canadensis, Lung (suis), Phytolacca Decandra, Symphytum Officinale, Aconitum Napellus, Arsenicum Album, Belladonna, Bryonia (alba), Causticum, Eupatorium Perfoliatum, Ferrum Phosphoricum, Gelsemium Sempervirens, Hypericum Perforatum, Kali Carbonicum, Lachesis Mutus, Natrum Sulphuricum, Phosphorus, Pulsatilla (pratensis), Rhus Tox, Silicea, Sulphur, Pyrogenium
Substance Name
Baptisia Tinctoria Root; Echinacea Angustifolia Whole; Lobelia Inflata Whole; Lomatium Dissectum Root; Goldenseal; Sus Scrofa Lung; Phytolacca Americana Root; Comfrey Root; Aconitum Napellus Whole; Arsenic Trioxide; Atropa Belladonna; Bryonia Alba Root; Causticum; Eupatorium Perfoliatum Flowering Top; Ferrosoferric Phosphate; Gelsemium Sempervirens Root; Hypericum Perforatum Whole; Potassium Carbonate; Lachesis Muta Venom; Sodium Sulfate; Phosphorus; Pulsatilla Pratensis Whole; Toxicodendron Pubescens Leaf; Silicon Dioxide; Sulfur; Rancid Beef
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with viral and bacterial infections, such as fever, irritated throat, and cough with tickle in the throat.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

Regulatory & Marketing

Labeler Name
Energique, Inc.
Product Type
Human Prescription Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
05-25-2021
End Marketing Date
05-08-2028
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 44911-0615-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Lymphastat, a human prescription drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains baptisia tinctoria root; echinacea angustifolia whole; lobelia inflata whole; lomatium dissectum root; goldenseal; sus scrofa lung; phytolacca americana root; comfrey root; aconitum napellus whole; arsenic trioxide; atropa belladonna; bryonia alba root; causticum; eupatorium perfoliatum flowering top; ferrosoferric phosphate; gelsemium sempervirens root; hypericum perforatum whole; potassium carbonate; lachesis muta venom; sodium sulfate; phosphorus; pulsatilla pratensis whole; toxicodendron pubescens leaf; silicon dioxide; sulfur; rancid beef 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 25, 2021.

How is this Energique, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911061501. 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:

10-Digit Format (5-4-1)
44911-0615-1
11-Digit CMS (5-4-2)
44911-0615-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.