Lymphastat Liquid
NDC Package 44911-0740-1

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 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 44911-0740.

Identification & Billing

NDC Package Code
44911-0740-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
44911-0740
11-Digit Billing Format
44911074001

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
Aconitum Napellus Whole; Arsenic Trioxide; Atropa Belladonna; Baptisia Tinctoria Root; Bryonia Alba Root; Causticum; Comfrey Root; Echinacea Angustifolia Whole; Eupatorium Perfoliatum Flowering Top; Ferrosoferric Phosphate; Gelsemium Sempervirens Root; Goldenseal; Hypericum Perforatum Whole; Lachesis Muta Venom; Lobelia Inflata Whole; Lomatium Dissectum Root; Phosphorus; Phytolacca Americana Root; Potassium Carbonate; Pulsatilla Pratensis Whole; Rancid Beef; Silicon Dioxide; Sodium Sulfate; Sulfur; Sus Scrofa Lung; Toxicodendron Pubescens Leaf
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
• 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.

Regulatory & Marketing

Labeler Name
Energique, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
01-07-2026
Listing Expiration
12-31-2027
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 44911-0740-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Lymphastat, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains aconitum napellus whole; arsenic trioxide; atropa belladonna; baptisia tinctoria root; bryonia alba root; causticum; comfrey root; echinacea angustifolia whole; eupatorium perfoliatum flowering top; ferrosoferric phosphate; gelsemium sempervirens root; goldenseal; hypericum perforatum whole; lachesis muta venom; lobelia inflata whole; lomatium dissectum root; phosphorus; phytolacca americana root; potassium carbonate; pulsatilla pratensis whole; rancid beef; silicon dioxide; sodium sulfate; sulfur; sus scrofa lung; 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 January 07, 2026. The current certification is valid through December 31, 2027.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911074001. 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)
44911-0740-1
11-Digit CMS (5-4-2)
44911-0740-01

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