44911-0456 NDC - LYMPHAPAR (ECHINACEA (ANGUSTIFOLIA), LYMPH NODE (SUIS), PHYTOLACCA DECANDRA, CONIUM MACULATUM, FERRUM IODATUM, HEPAR SULPHURIS CALCAREUM , KALI MURIATICUM, LACHESIS MUTUS, SILICEA)

Drug Information

Product NDC: 44911-0456

Proprietary Name: Lymphapar

Non Proprietary Name: Echinacea (Angustifolia), Lymph Node (Suis), Phytolacca Decandra, Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum , Kali Muriaticum, Lachesis Mutus, Silicea

Active Ingredient(s):
  • 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA;
  • 6 [hp_X]/mL SUS SCROFA LYMPH;
  • 6 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 12 [hp_X]/mL CONIUM MACULATUM FLOWERING TOP;
  • 12 [hp_X]/mL FERROUS IODIDE;
  • 12 [hp_X]/mL CALCIUM SULFIDE;
  • 12 [hp_X]/mL POTASSIUM CHLORIDE;
  • 12 [hp_X]/mL LACHESIS MUTA VENOM;
  • 12 [hp_X]/mL SILICON DIOXIDE


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:5/14/2018

Package Information

No. Package Code Package Description Billing Unit
144911-0456-130 mL in 1 BOTTLE, DROPPER (44911-0456-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC44911-0456The 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), Lymph Node (Suis), Phytolacca Decandra, Conium Maculatum, Ferrum Iodatum, Hepar Sulphuris Calcareum , Kali Muriaticum, Lachesis Mutus, 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 DATE5/14/2018This 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 NAMEECHINACEA ANGUSTIFOLIA; SUS SCROFA LYMPH; PHYTOLACCA AMERICANA ROOT; CONIUM MACULATUM FLOWERING TOP; FERROUS IODIDE; CALCIUM SULFIDE; POTASSIUM CHLORIDE; LACHESIS MUTA VENOM; SILICON DIOXIDEThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH3; 6; 6; 12; 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 

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