50114-8200 NDC - LYMPHOMYOSOT X (ARANEUS DIADEMATUS, TRIBASIC CALCIUM PHOSPHATE, EQUISETUM HYEMALE, FERROUS IODIDE,FUMARIA OFFICINALIS FLOWERING TOP, GENTIANA LUTEA ROOT, GERANIUM ROBERTIANUM, MYOSOTIS ARVENSIS, NASTURTIUM OFFICINALE, SODIUM SULFATE, PINUS SYLVESTRIS LEAFY TWIG,SMILAX REGELII ROOT, SCROPHULARIA NODOSA, TEUCRIUM SCORODONIA FLOWERING TOP, THYROID, UNSPECIFIED ANDVERONICA OFFICINALIS FLOWERING TOP)

Drug Information

Product NDC: 50114-8200

Proprietary Name: Lymphomyosot X

Non Proprietary Name: ARANEUS DIADEMATUS, TRIBASIC CALCIUM PHOSPHATE, EQUISETUM HYEMALE, FERROUS IODIDE,FUMARIA OFFICINALIS FLOWERING TOP, GENTIANA LUTEA ROOT, GERANIUM ROBERTIANUM, MYOSOTIS ARVENSIS, NASTURTIUM OFFICINALE, SODIUM SULFATE, PINUS SYLVESTRIS LEAFY TWIG,SMILAX REGELII ROOT, SCROPHULARIA NODOSA, TEUCRIUM SCORODONIA FLOWERING TOP, THYROID, UNSPECIFIED andVERONICA OFFICINALIS FLOWERING TOP

Active Ingredient(s):
  • 6 [hp_X]/1.1mL ARANEUS DIADEMATUS;
  • 12 [hp_X]/1.1mL TRIBASIC CALCIUM PHOSPHATE;
  • 12 [hp_X]/1.1mL EQUISETUM HYEMALE;
  • 3 [hp_X]/1.1mL FERROUS IODIDE;
  • 4 [hp_X]/1.1mL FUMARIA OFFICINALIS FLOWERING TOP;
  • 5 [hp_X]/1.1mL GENTIANA LUTEA ROOT;
  • 4 [hp_X]/1.1mL GERANIUM ROBERTIANUM;
  • 3 [hp_X]/1.1mL MYOSOTIS ARVENSIS;
  • 4 [hp_X]/1.1mL NASTURTIUM OFFICINALE;
  • 4 [hp_X]/1.1mL SODIUM SULFATE;
  • 4 [hp_X]/1.1mL PINUS SYLVESTRIS LEAFY TWIG;
  • 6 [hp_X]/1.1mL SMILAX REGELII ROOT;
  • 3 [hp_X]/1.1mL SCROPHULARIA NODOSA;
  • 3 [hp_X]/1.1mL TEUCRIUM SCORODONIA FLOWERING TOP;
  • 12 [hp_X]/1.1mL THYROID, UNSPECIFIED;
  • 3 [hp_X]/1.1mL VERONICA OFFICINALIS FLOWERING TOP


Administration Route(s): INTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUS

Dosage Form(s): INJECTION

Pharmacy Class(es):
  • Blood Coagulation Factor [EPC];
  • Increased Coagulation Factor Activity [PE];
  • Calcium [CS];
  • Cations;
  • Divalent [CS]

Labeler Information

Labeler Name: MediNatura
Product Type: HUMAN PRESCRIPTION DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:4/1/2010

Package Information

No. Package Code Package Description Billing Unit
150114-8200-110 AMPULE in 1 CARTON (50114-8200-1) > 1.1 mL in 1 AMPULEML
250114-8200-33 AMPULE in 1 CARTON (50114-8200-3) > 1.1 mL in 1 AMPULE

NDC Record

Field Name Field Value Definition
PRODUCT NDC50114-8200The 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 PRESCRIPTION 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 NAMELymphomyosot XThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEARANEUS DIADEMATUS, TRIBASIC CALCIUM PHOSPHATE, EQUISETUM HYEMALE, FERROUS IODIDE,FUMARIA OFFICINALIS FLOWERING TOP, GENTIANA LUTEA ROOT, GERANIUM ROBERTIANUM, MYOSOTIS ARVENSIS, NASTURTIUM OFFICINALE, SODIUM SULFATE, PINUS SYLVESTRIS LEAFY TWIG,SMILAX REGELII ROOT, SCROPHULARIA NODOSA, TEUCRIUM SCORODONIA FLOWERING TOP, THYROID, UNSPECIFIED andVERONICA OFFICINALIS FLOWERING TOPThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMEINJECTIONThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEINTRADERMAL; INTRAMUSCULAR; INTRAVENOUS; SUBCUTANEOUSThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE4/1/2010This 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 NAMEMediNaturaName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARANEUS DIADEMATUS; TRIBASIC CALCIUM PHOSPHATE; EQUISETUM HYEMALE; FERROUS IODIDE; FUMARIA OFFICINALIS FLOWERING TOP; GENTIANA LUTEA ROOT; GERANIUM ROBERTIANUM; MYOSOTIS ARVENSIS; NASTURTIUM OFFICINALE; SODIUM SULFATE; PINUS SYLVESTRIS LEAFY TWIG; SMILAX REGELII ROOT; SCROPHULARIA NODOSA; TEUCRIUM SCORODONIA FLOWERING TOP; THYROID, UNSPECIFIED; VERONICA OFFICINALIS FLOWERING TOPThis is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
ACTIVE NUMERATOR STRENGTH6; 12; 12; 3; 4; 5; 4; 3; 4; 4; 4; 6; 3; 3; 12; 3 
ACTIVE INGRED UNIT[hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL; [hp_X]/1.1mL 
PHARM CLASSESBlood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [CS],Cations, Divalent [CS] 

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