Thyro-chord Liquid
NDC 64578-0076

View dosage, usage, ingredients, routes, and UNII mappings.

Product Information

Thyro-chord (homeopathic liquid) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energetix Corporation. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 64578-0076 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
64578-0076
Proprietary Name:
Thyro-chord
Non-Proprietary Name: [1]
Homeopathic Liquid
Substance Name: [2]
.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 Oxide
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Code:
64578
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-08-2017
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 64578-0076?

The NDC code 64578-0076 is assigned by the FDA to the product Thyro-chord. It is commonly known by its generic name, homeopathic liquid. This pharmaceutical product is labeled by Energetix Corporation and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 64578-0076-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are Active Ingredients of this product?

An 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.
  • .ALPHA.-KETOGLUTARIC ACID 12 [hp_X]/59.1mL - A family of compounds containing an oxo group with the general structure of 1,5-pentanedioic acid. (From Lehninger, Principles of Biochemistry, 1982, p442)
  • ACETIC ACID 15 [hp_X]/59.1mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
  • AMMONIUM CHLORIDE 15 [hp_X]/59.1mL - An acidifying agent that has expectorant and diuretic effects. Also used in etching and batteries and as a flux in electroplating.
  • ASPARAGUS 12 [hp_X]/59.1mL
  • CHELIDONIUM MAJUS 4 [hp_X]/59.1mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
  • COENZYME A 12 [hp_X]/59.1mL - Venoms from jellyfish; CORALS; SEA ANEMONES; etc. They contain hemo-, cardio-, dermo- , and neuro-toxic substances and probably ENZYMES. They include palytoxin, sarcophine, and anthopleurine.
  • COPPER 15 [hp_X]/59.1mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • ECHINACEA ANGUSTIFOLIA 4 [hp_X]/59.1mL - A genus of perennial herbs used topically and internally. It contains echinacoside, GLYCOSIDES; INULIN; isobutyl amides, resin, and SESQUITERPENES.
  • FERROUS IODIDE 12 [hp_X]/59.1mL
  • FUCUS VESICULOSUS 6 [hp_X]/59.1mL - A genus of BROWN ALGAE in the family Fucaceae. It is found in temperate, marine intertidal areas along rocky coasts and is a source of ALGINATES. Some species of Fucus are referred to as KELP.
  • FUMARIC ACID 12 [hp_X]/59.1mL - see also record for ferrous fumarate; use FUMARATES for general fumaric acid esters
  • GENTIANA LUTEA ROOT 4 [hp_X]/59.1mL
  • GLYCYRRHIZA GLABRA 4 [hp_X]/59.1mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
  • GOLD 15 [hp_X]/59.1mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
  • IODINE 8 [hp_X]/59.1mL - A nonmetallic element of the halogen group that is represented by the atomic symbol I, atomic number 53, and atomic weight of 126.90. It is a nutritionally essential element, especially important in thyroid hormone synthesis. In solution, it has anti-infective properties and is used topically.
  • MERCURIUS SOLUBILIS 15 [hp_X]/59.1mL
  • NADIDE 12 [hp_X]/59.1mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/59.1mL
  • PALLADIUM 15 [hp_X]/59.1mL - A chemical element having an atomic weight of 106.4, atomic number of 46, and the symbol Pd. It is a white, ductile metal resembling platinum, and following it in abundance and importance of applications. It is used in dentistry in the form of gold, silver, and copper alloys.
  • PERSICARIA PUNCTATA 12 [hp_X]/59.1mL
  • PHOSPHORIC ACID 12 [hp_X]/59.1mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • POTASSIUM IODIDE 12 [hp_X]/59.1mL - An inorganic compound that is used as a source of iodine in thyrotoxic crisis and in the preparation of thyrotoxic patients for thyroidectomy. (From Dorland, 27th ed)
  • PULSATILLA VULGARIS 12 [hp_X]/59.1mL
  • RANCID BEEF 12 [hp_X]/59.1mL
  • SAGE 8 [hp_X]/59.1mL
  • SILICON DIOXIDE 12 [hp_X]/59.1mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
  • SILVER 15 [hp_X]/59.1mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
  • SODIUM DIETHYL OXALACETATE 12 [hp_X]/59.1mL
  • SODIUM PYRUVATE 12 [hp_X]/59.1mL
  • SUCCINIC ACID 12 [hp_X]/59.1mL - A water-soluble, colorless crystal with an acid taste that is used as a chemical intermediate, in medicine, the manufacture of lacquers, and to make perfume esters. It is also used in foods as a sequestrant, buffer, and a neutralizing agent. (Hawley's Condensed Chemical Dictionary, 12th ed, p1099; McGraw-Hill Dictionary of Scientific and Technical Terms, 4th ed, p1851)
  • THYROID, UNSPECIFIED 9 [hp_X]/59.1mL
  • TIN 15 [hp_X]/59.1mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
  • VANADIUM 15 [hp_X]/59.1mL - A metallic element with the atomic symbol V, atomic number 23, and atomic weight 50.94. It is used in the manufacture of vanadium steel. Prolonged exposure can lead to chronic intoxication caused by absorption usually via the lungs.
  • ZINC OXIDE 15 [hp_X]/59.1mL - A mild astringent and topical protectant with some antiseptic action. It is also used in bandages, pastes, ointments, dental cements, and as a sunblock.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? An 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.
What kind of product is this? Indicates 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? Product 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".