Thyropath Liquid
NDC 64578-0133

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 64578-0133?
  4. Active Ingredients
  5. Active Ingredients UNII Codes
  6. Inactive Ingredients UNII Codes
  7. Pharmacologic Classes

Product Information

Thyropath (avena sativa, borago officinalis, calcarea carbonica, chelidonium majus, ferrum iodatum, fucus vesiculosus, glandula suprarenalis suis, hepar suis, iodium, kali iodatum, phosphoricum acidum, pituitarum posterium (bovine), pyridoxinum hydrochloricum, thyroidinum (bovine), zincum metallicum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energetix Corporation. This medication is typically used as a analogs/derivatives [chemical/ingredient]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 64578-0133 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
64578-0133
Proprietary Name:
Thyropath
Non-Proprietary Name: [1]
Avena Sativa, Borago Officinalis, Calcarea Carbonica, Chelidonium Majus, Ferrum Iodatum, Fucus Vesiculosus, Glandula Suprarenalis Suis, Hepar Suis, Iodium, Kali Iodatum, Phosphoricum Acidum, Pituitarum Posterium (bovine), Pyridoxinum Hydrochloricum, Thyroidinum (bovine), Zincum Metallicum
Substance Name: [2]
Avena Sativa Flowering Top; Borage; Bos Taurus Pituitary Gland, Posterior; Chelidonium Majus; Ferrous Iodide; Fucus Vesiculosus; Iodine; Oyster Shell Calcium Carbonate, Crude; Phosphoric Acid; Pork Liver; Potassium Iodide; Pyridoxine Hydrochloride; Sus Scrofa Adrenal Gland; Thyroid, Bovine; Zinc
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 Name: [5]
Energetix Corporation
Labeler Code:
64578
Product Label ID:
f8ec1c51-520c-4bbe-8701-e875ea88a628
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
11-15-2016
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 64578-0133?

The NDC code 64578-0133 is assigned by the FDA to the product Thyropath. It is commonly known by its generic name, avena sativa, borago officinalis, calcarea carbonica, chelidonium majus, ferrum iodatum, fucus vesiculosus, glandula suprarenalis suis, hepar suis, iodium, kali iodatum, phosphoricum acidum, pituitarum posterium (bovine), pyridoxinum hydrochloricum, thyroidinum (bovine), zincum metallicum. 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: 64578-0133-1. 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.
  • AVENA SATIVA FLOWERING TOP 4 [hp_X]/mL
  • BORAGE 6 [hp_X]/mL
  • BOS TAURUS PITUITARY GLAND, POSTERIOR 12 [hp_X]/mL
  • CHELIDONIUM MAJUS 4 [hp_X]/mL - 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).
  • FERROUS IODIDE 12 [hp_X]/mL
  • FUCUS VESICULOSUS 4 [hp_X]/mL - 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.
  • IODINE 12 [hp_X]/mL - 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.
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • PORK LIVER 9 [hp_X]/mL
  • POTASSIUM IODIDE 12 [hp_X]/mL - 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)
  • PYRIDOXINE HYDROCHLORIDE 10 [hp_X]/mL - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
  • SUS SCROFA ADRENAL GLAND 9 [hp_X]/mL
  • THYROID, BOVINE 9 [hp_X]/mL
  • ZINC 12 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

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?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients 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".