44911-0707 NDC - LYMPHAPAR (ECHINACEA (ANGUSTIFOLIA), CALENDULA OFFICINALIS, LYMPH NODE (SUIS), PHYTOLACCA DECANDRA, ASTERIAS RUBENS, BARYTA CARBONICA, CONIUM MACULATUM, FERRUM IODATUM, HEPAR SULPHURIS CALCAREUM , KALI MURIATICUM, LACHESIS MUTUS, SCROPHULARIA NODOSA, SILICEA)

Drug Information

  • Product NDC: 44911-0707
  • Proprietary Name: Lymphapar
  • Non Proprietary Name: Echinacea (Angustifolia), Calendula Officinalis, Lymph Node (Suis), Phytolacca Decandra, Asterias Rubens, Baryta Carbonica, Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum , Kali Muriaticum, Lachesis Mutus, Scrophularia Nodosa, Silicea
  • Active Ingredient(s): 12 [hp_X]/mL ASTERIAS RUBENS; 12 [hp_X]/mL BARIUM CARBONATE; 12 [hp_X]/mL CALCIUM SULFIDE; 6 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP; 12 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 12 [hp_X]/mL FERROUS IODIDE; 12 [hp_X]/mL LACHESIS MUTA VENOM; 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 12 [hp_X]/mL POTASSIUM CHLORIDE; 12 [hp_X]/mL SCROPHULARIA NODOSA WHOLE; 12 [hp_X]/mL SILICON DIOXIDE; 6 [hp_X]/mL SUS SCROFA LYMPH
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Increased Large Intestinal Motility [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Potassium Compounds [CS]; Potassium Salt [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Energique, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/20/2024

Package Information

No. Package Code Package Description Billing Unit
144911-0707-130 mL in 1 BOTTLE, DROPPER (44911-0707-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0707The 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 NAMELymphaparThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEEchinacea (Angustifolia), Calendula Officinalis, Lymph Node (Suis), Phytolacca Decandra, Asterias Rubens, Baryta Carbonica, Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum , Kali Muriaticum, Lachesis Mutus, Scrophularia Nodosa, SiliceaThe 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 DATE9/20/2024This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NAMEASTERIAS RUBENS; BARIUM CARBONATE; CALCIUM SULFIDE; CALENDULA OFFICINALIS FLOWERING TOP; CONIUM MACULATUM FLOWERING TOP; ECHINACEA ANGUSTIFOLIA WHOLE; FERROUS IODIDE; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; SCROPHULARIA NODOSA WHOLE; SILICON DIOXIDE; SUS SCROFA LYMPHAn active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH12; 12; 12; 6; 12; 3; 12; 12; 6; 12; 12; 12; 6 
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 
PHARM CLASSESIncreased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] 

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This page was last updated on: 7/4/2025

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