64578-0076 NDC - THYRO-CHORD (HOMEOPATHIC LIQUID)

Drug Information

Product NDC: 64578-0076

Proprietary Name: Thyro-Chord

Non Proprietary Name: Homeopathic Liquid

Active Ingredient(s):
  • 12 [hp_X]/59.1mL .ALPHA.-KETOGLUTARIC ACID;
  • 15 [hp_X]/59.1mL ACETIC ACID;
  • 15 [hp_X]/59.1mL AMMONIUM CHLORIDE;
  • 12 [hp_X]/59.1mL ASPARAGUS;
  • 4 [hp_X]/59.1mL CHELIDONIUM MAJUS;
  • 12 [hp_X]/59.1mL COENZYME A;
  • 15 [hp_X]/59.1mL COPPER;
  • 4 [hp_X]/59.1mL ECHINACEA ANGUSTIFOLIA;
  • 12 [hp_X]/59.1mL FERROUS IODIDE;
  • 6 [hp_X]/59.1mL FUCUS VESICULOSUS;
  • 12 [hp_X]/59.1mL FUMARIC ACID;
  • 4 [hp_X]/59.1mL GENTIANA LUTEA ROOT;
  • 4 [hp_X]/59.1mL GLYCYRRHIZA GLABRA;
  • 15 [hp_X]/59.1mL GOLD;
  • 8 [hp_X]/59.1mL IODINE;
  • 15 [hp_X]/59.1mL MERCURIUS SOLUBILIS;
  • 12 [hp_X]/59.1mL NADIDE;
  • 12 [hp_X]/59.1mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 15 [hp_X]/59.1mL PALLADIUM;
  • 12 [hp_X]/59.1mL PERSICARIA PUNCTATA;
  • 12 [hp_X]/59.1mL PHOSPHORIC ACID;
  • 12 [hp_X]/59.1mL POTASSIUM IODIDE;
  • 12 [hp_X]/59.1mL PULSATILLA VULGARIS;
  • 12 [hp_X]/59.1mL RANCID BEEF;
  • 8 [hp_X]/59.1mL SAGE;
  • 12 [hp_X]/59.1mL SILICON DIOXIDE;
  • 15 [hp_X]/59.1mL SILVER;
  • 12 [hp_X]/59.1mL SODIUM DIETHYL OXALACETATE;
  • 12 [hp_X]/59.1mL SODIUM PYRUVATE;
  • 12 [hp_X]/59.1mL SUCCINIC ACID;
  • 9 [hp_X]/59.1mL THYROID, UNSPECIFIED;
  • 15 [hp_X]/59.1mL TIN;
  • 15 [hp_X]/59.1mL VANADIUM;
  • 15 [hp_X]/59.1mL ZINC OXIDE


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Copper Absorption Inhibitor [EPC];
  • Copper [CS];
  • Copper-containing Intrauterine Device [EPC];
  • Decreased Copper Ion Absorption [PE];
  • Decreased Embryonic Implantation [PE];
  • Decreased Sperm Motility [PE];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Inhibit Ovum Fertilization [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Standardized Chemical Allergen [EPC];
  • Vegetable Proteins [CS]

Labeler Information

Labeler Name: Energetix Corporation
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:9/8/2017

Package Information

No. Package Code Package Description Billing Unit
164578-0076-159.1 mL in 1 BOTTLE, DROPPER (64578-0076-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC64578-0076The 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 NAMEThyro-ChordThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEHomeopathic LiquidThe 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 DATE9/8/2017This 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 NAMEEnergetix CorporationName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.ALPHA.-KETOGLUTARIC ACID; ACETIC ACID; AMMONIUM CHLORIDE; ASPARAGUS; CHELIDONIUM MAJUS; COENZYME A; COPPER; ECHINACEA ANGUSTIFOLIA; FERROUS IODIDE; FUCUS VESICULOSUS; FUMARIC ACID; GENTIANA LUTEA ROOT; GLYCYRRHIZA GLABRA; GOLD; IODINE; MERCURIUS SOLUBILIS; NADIDE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PALLADIUM; PERSICARIA PUNCTATA; PHOSPHORIC ACID; POTASSIUM IODIDE; PULSATILLA VULGARIS; RANCID BEEF; SAGE; SILICON DIOXIDE; SILVER; SODIUM DIETHYL OXALACETATE; SODIUM PYRUVATE; SUCCINIC ACID; THYROID, UNSPECIFIED; TIN; VANADIUM; ZINC OXIDEAn 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; 15; 15; 12; 4; 12; 15; 4; 12; 6; 12; 4; 4; 15; 8; 15; 12; 12; 15; 12; 12; 12; 12; 12; 8; 12; 15; 12; 12; 12; 9; 15; 15; 15 
ACTIVE INGRED UNIT[hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL; [hp_X]/59.1mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Dietary Proteins [CS], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Inhibit Ovum Fertilization [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Standardized Chemical Allergen [EPC], Vegetable Proteins [CS] 

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