44911-0120 NDC - LYMPHDRAINEX (GERANIUM ROBERTIANUM, NASTURTIUM AQUATICUM, ALOE SOCOTRINA, MYOSOTIS ARVENSIS, SCROPHULARIA NODOSA, TEUCRIUM SCORODONIA, APIS MELLIFICA, EQUISETUM HYEMALE, FUMARIA OFFICINALIS, NATRUM SULPHURICUM, PHYTOLACCA DECANDRA, PINUS SYLVESTRIS, VERONICA OFFICINALIS, GENTIANA LUTEA, JUGLANS REGIA, SARSAPARILLA (SMILAX REGELII) BARYTA CARBONICA, HEPAR SULPHURIS CALCAREUM, MERCURIUS CYANATUS, FERRUM IODATUM, ARANEA DIADEMA, CALCAREA PHOSPHORICA, PARATHYROID GLAND (BOVINE), THYMUS (SUIS), THYROIDINUM (SUIS))

Drug Information

Product NDC: 44911-0120

Proprietary Name: Lymphdrainex

Non Proprietary Name: Geranium Robertianum, Nasturtium Aquaticum, Aloe Socotrina, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia, Apis Mellifica, Equisetum Hyemale, Fumaria Officinalis, Natrum Sulphuricum, Phytolacca Decandra, Pinus Sylvestris, Veronica Officinalis, Gentiana Lutea, Juglans Regia, Sarsaparilla (Smilax Regelii) Baryta Carbonica, Hepar Sulphuris Calcareum, Mercurius Cyanatus, Ferrum Iodatum, Aranea Diadema, Calcarea Phosphorica, Parathyroid Gland (Bovine), Thymus (Suis), Thyroidinum (Suis)

Active Ingredient(s):
  • 3 [hp_X]/mL GERANIUM ROBERTIANUM;
  • 3 [hp_X]/mL NASTURTIUM OFFICINALE;
  • 3 [hp_X]/mL ALOE;
  • 3 [hp_X]/mL MYOSOTIS ARVENSIS;
  • 3 [hp_X]/mL SCROPHULARIA NODOSA;
  • 3 [hp_X]/mL TEUCRIUM SCORODONIA FLOWERING TOP;
  • 4 [hp_X]/mL APIS MELLIFERA;
  • 4 [hp_X]/mL EQUISETUM HYEMALE;
  • 4 [hp_X]/mL FUMARIA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/mL SODIUM SULFATE;
  • 4 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 4 [hp_X]/mL PINUS SYLVESTRIS LEAFY TWIG;
  • 4 [hp_X]/mL VERONICA OFFICINALIS FLOWERING TOP;
  • 5 [hp_X]/mL GENTIANA LUTEA ROOT;
  • 5 [hp_X]/mL JUGLANS REGIA FRUIT RIND, IMMATURE;
  • 5 [hp_X]/mL JUGLANS REGIA LEAF;
  • 6 [hp_X]/mL SMILAX REGELII ROOT;
  • 8 [hp_X]/mL BARIUM CARBONATE;
  • 8 [hp_X]/mL CALCIUM SULFIDE;
  • 8 [hp_X]/mL MERCURIC CYANIDE;
  • 8 [hp_X]/mL FERROUS IODIDE;
  • 12 [hp_X]/mL ARANEUS DIADEMATUS;
  • 12 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE;
  • 12 [hp_X]/mL BOS TAURUS PARATHYROID GLAND;
  • 12 [hp_X]/mL SUS SCROFA THYMUS;
  • 12 [hp_X]/mL SUS SCROFA THYROID


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/27/2014
End Marketing Date:7/11/2022

Package Information

No. Package Code Package Description Billing Unit
144911-0120-160 mL in 1 BOTTLE, DROPPER (44911-0120-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0120The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
PROPRIETARY NAMELymphdrainexThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGeranium Robertianum, Nasturtium Aquaticum, Aloe Socotrina, Myosotis Arvensis, Scrophularia Nodosa, Teucrium Scorodonia, Apis Mellifica, Equisetum Hyemale, Fumaria Officinalis, Natrum Sulphuricum, Phytolacca Decandra, Pinus Sylvestris, Veronica Officinalis, Gentiana Lutea, Juglans Regia, Sarsaparilla (Smilax Regelii) Baryta Carbonica, Hepar Sulphuris Calcareum, Mercurius Cyanatus, Ferrum Iodatum, Aranea Diadema, Calcarea Phosphorica, Parathyroid Gland (Bovine), Thymus (Suis), Thyroidinum (Suis)The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/27/2014This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE7/11/2022This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
LABELER NAMEEnergique, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEGERANIUM ROBERTIANUM; NASTURTIUM OFFICINALE; ALOE; MYOSOTIS ARVENSIS; SCROPHULARIA NODOSA; 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; JUGLANS REGIA FRUIT RIND, IMMATURE; JUGLANS REGIA LEAF; SMILAX REGELII ROOT; BARIUM CARBONATE; CALCIUM SULFIDE; MERCURIC CYANIDE; FERROUS IODIDE; ARANEUS DIADEMATUS; TRIBASIC CALCIUM PHOSPHATE; BOS TAURUS PARATHYROID GLAND; SUS SCROFA THYMUS; SUS SCROFA THYROIDThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 3; 3; 3; 3; 3; 4; 4; 4; 4; 4; 4; 4; 5; 5; 5; 6; 8; 8; 8; 8; 12; 12; 12; 12; 12 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 

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This page was last updated on: 9/13/2019