43406-0679 NDC - VERMASODE (ARTEMISIA VULGARIS, CHELIDONIUM MAJUS, GRANATUM, SPIGELIA ANTHELMIA, RATANHIA, ARSENICUM ALBUM, FERRUM METALLICUM, CALCAREA CARBONICA, CINA, GAERTNER BACILLUS, GRAPHITES, MERCURIUS DULCIS, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, VERMIN NOSODE)

Drug Information

Product NDC: 43406-0679

Proprietary Name: Vermasode

Non Proprietary Name: Artemisia Vulgaris, Chelidonium Majus, Granatum, Spigelia Anthelmia, Ratanhia, Arsenicum Album, Ferrum Metallicum, Calcarea Carbonica, Cina, Gaertner Bacillus, Graphites, Mercurius Dulcis, Natrum Muriaticum, Natrum Phosphoricum, Vermin Nosode

Active Ingredient(s):
  • 6 [hp_X]/mL ARSENIC TRIOXIDE;
  • 12 [hp_X]/mL ARTEMISIA CINA PRE-FLOWERING TOP;
  • 4 [hp_X]/mL ARTEMISIA VULGARIS ROOT;
  • 12 [hp_X]/mL CALOMEL;
  • 4 [hp_X]/mL CHELIDONIUM MAJUS WHOLE;
  • 12 [hp_X]/mL GRAPHITE;
  • 9 [hp_X]/mL IRON;
  • 4 [hp_X]/mL KRAMERIA LAPPACEA ROOT;
  • 12 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 4 [hp_X]/mL PUNICA GRANATUM ROOT BARK;
  • 12 [hp_X]/mL SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS;
  • 12 [hp_X]/mL SODIUM CHLORIDE;
  • 12 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE;
  • 4 [hp_X]/mL SPIGELIA ANTHELMIA WHOLE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Labeler Information

Labeler Name: Natural Creations, Inc
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/13/2018

Package Information

No. Package Code Package Description Billing Unit
143406-0679-130 mL in 1 BOTTLE, DROPPER (43406-0679-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43406-0679The 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 NAMEVermasodeThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEArtemisia Vulgaris, Chelidonium Majus, Granatum, Spigelia Anthelmia, Ratanhia, Arsenicum Album, Ferrum Metallicum, Calcarea Carbonica, Cina, Gaertner Bacillus, Graphites, Mercurius Dulcis, Natrum Muriaticum, Natrum Phosphoricum, Vermin NosodeThe 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 DATE6/13/2018This 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 NAMENatural Creations, IncName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARSENIC TRIOXIDE; ARTEMISIA CINA PRE-FLOWERING TOP; ARTEMISIA VULGARIS ROOT; CALOMEL; CHELIDONIUM MAJUS WHOLE; GRAPHITE; IRON; KRAMERIA LAPPACEA ROOT; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PUNICA GRANATUM ROOT BARK; SALMONELLA ENTERICA ENTERICA SEROVAR ENTERITIDIS; SODIUM CHLORIDE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SPIGELIA ANTHELMIA WHOLEAn 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 STRENGTH6; 12; 4; 12; 4; 12; 9; 4; 12; 4; 12; 12; 12; 4 
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 

Download Record

Download this NDC record in Text format: Export

Download this NDC record in Excel (CSV) format: Export

Download this NDC record in XML format: Export

This page was last updated on: 2/1/2023