Lymphdrainex Liquid
NDC Package 44911-0647-1

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

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

Lymphdrainex (geranium robertianum, nasturtium aquaticum, scrophularia nodosa, teucrium scorodonia, apis mellifica, equisetum hyemale, fumaria officinalis, natrum sulphuricum, phytolacca decandra, pinus sylvestris, veronica officinalis, aloe, gentiana lutea, juglans regia, myosotis arvensis, sarsaparilla (smilax regelii), baryta carbonica, hepar sulphuris calcareum, mercurius cyanatus, ferrum iodatum, aranea diadema, calcarea phosphorica, parathyroid gland (bovine), thymus (suis), thyroidinum (suis)) liquids May temporarily relieve symptoms associated with lymphatic congestion, such as tendency to catch colds, fluid retention, and fatique.****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 44911-0647.

Identification & Billing

NDC Package Code
44911-0647-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
44911-0647
11-Digit Billing Format
44911064701

Clinical Specifications

Proprietary Name
Lymphdrainex
Non-Proprietary Name
Geranium Robertianum, Nasturtium Aquaticum, Scrophularia Nodosa, Teucrium Scorodonia, Apis Mellifica, Equisetum Hyemale, Fumaria Officinalis, Natrum Sulphuricum, Phytolacca Decandra, Pinus Sylvestris, Veronica Officinalis, Aloe, Gentiana Lutea, Juglans Regia, Myosotis Arvensis, Sarsaparilla (smilax Regelii), Baryta Carbonica, Hepar Sulphuris Calcareum, Mercurius Cyanatus, Ferrum Iodatum, Aranea Diadema, Calcarea Phosphorica, Parathyroid Gland (bovine), Thymus (suis), Thyroidinum (suis)
Substance Name
Geranium Robertianum; Nasturtium Officinale; Teucrium Scorodonia Flowering Top; Apis Mellifera; Equisetum Hyemale; Fumaria Officinalis Flowering Top; Sodium Sulfate; Phytolacca Americana Root; Pinus Sylvestris Leafy Twig; Veronica Officinalis Flowering Top; Gentiana Lutea Root; Smilax Ornata Root; Barium Carbonate; Calcium Sulfide; Mercuric Cyanide; Scrophularia Nodosa Whole; Aloe; Ferrous Iodide; Myosotis Arvensis Whole; Araneus Diadematus; Tribasic Calcium Phosphate; Juglans Regia Fruit Rind, Immature; Bos Taurus Parathyroid Gland; Sus Scrofa Thymus; Sus Scrofa Thyroid
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)
Pharmacologic Class
Usage Information
May temporarily relieve symptoms associated with lymphatic congestion, such as tendency to catch colds, fluid retention, and fatique.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated. May temporarily relieve symptoms associated with lymphatic congestion, such as tendency to catch colds, fluid retention, and fatique.****Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

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
10-06-2021
End Marketing Date
10-06-2026
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 44911-0647-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Lymphdrainex, a human over the counter drug labeled by Energique, Inc.. This liquid is formulated for oral use and contains geranium robertianum; nasturtium officinale; teucrium scorodonia flowering top; apis mellifera; equisetum hyemale; fumaria officinalis flowering top; sodium sulfate; phytolacca americana root; pinus sylvestris leafy twig; veronica officinalis flowering top; gentiana lutea root; smilax ornata root; barium carbonate; calcium sulfide; mercuric cyanide; scrophularia nodosa whole; aloe; ferrous iodide; myosotis arvensis whole; araneus diadematus; tribasic calcium phosphate; juglans regia fruit rind, immature; bos taurus parathyroid gland; sus scrofa thymus; sus scrofa thyroid 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 October 06, 2021.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 44911064701. 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)
44911-0647-1
11-Digit CMS (5-4-2)
44911-0647-01

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