NDC 64578-0064 Hepata-chord

Homeopathic Liquid Liquid Oral - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
64578-0064
Proprietary Name:
Hepata-chord
Non-Proprietary Name: [1]
Homeopathic Liquid
Substance Name: [2]
Acetic Acid; Aluminum Oxide; Arctium Lappa Root; Aspirin; Benzene; Berberis Vulgaris Root Bark; Bos Taurus Hypothalamus; Centella Asiatica; Chelidonium Majus; Chelone Glabra; Chloramphenicol; Chlorpromazine; Cholesterol; Cortisone Acetate; Estrone; Gamboge; Kerosene; Milk Thistle; Paraffin; Phenacetin; Phosphorus; Pork Liver; Silicon Dioxide; Sodium Sulfate; Taraxacum Officinale; Thyroid, Unspecified
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
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 Name: [5]
    Energetix Corp
    Labeler Code:
    64578
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    11-17-2014
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 64578-0064-1

    Package Description: 59.1 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 64578-0064?

    The NDC code 64578-0064 is assigned by the FDA to the product Hepata-chord which is a human over the counter drug product labeled by Energetix Corp. The generic name of Hepata-chord is homeopathic liquid. The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 64578-0064-1 59.1 ml in 1 bottle, dropper . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are Hepata-chord Active Ingredients?

    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.
    • ACETIC ACID 18 [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)
    • ALUMINUM OXIDE 18 [hp_X]/59.1mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
    • ARCTIUM LAPPA ROOT 4 [hp_X]/59.1mL
    • ASPIRIN 18 [hp_X]/59.1mL - The prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)
    • BENZENE 12 [hp_X]/59.1mL - Toxic, volatile, flammable liquid hydrocarbon byproduct of coal distillation. It is used as an industrial solvent in paints, varnishes, lacquer thinners, gasoline, etc. Benzene causes central nervous system damage acutely and bone marrow damage chronically and is carcinogenic. It was formerly used as parasiticide.
    • BERBERIS VULGARIS ROOT BARK 4 [hp_X]/59.1mL
    • BOS TAURUS HYPOTHALAMUS 12 [hp_X]/59.1mL
    • CENTELLA ASIATICA 5 [hp_X]/59.1mL - A plant of the family APIACEAE which is the source of asiatic acid and asiaticoside. Centella asiatica (L.) Urb. = Hydrocotyle asiatica L. is known for effect on peripheral circulation.
    • 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).
    • CHELONE GLABRA 12 [hp_X]/59.1mL
    • CHLORAMPHENICOL 18 [hp_X]/59.1mL - An antibiotic first isolated from cultures of Streptomyces venequelae in 1947 but now produced synthetically. It has a relatively simple structure and was the first broad-spectrum antibiotic to be discovered. It acts by interfering with bacterial protein synthesis and is mainly bacteriostatic. (From Martindale, The Extra Pharmacopoeia, 29th ed, p106)
    • CHLORPROMAZINE 18 [hp_X]/59.1mL - The prototypical phenothiazine antipsychotic drug. Like the other drugs in this class chlorpromazine's antipsychotic actions are thought to be due to long-term adaptation by the brain to blocking DOPAMINE RECEPTORS. Chlorpromazine has several other actions and therapeutic uses, including as an antiemetic and in the treatment of intractable hiccup.
    • CHOLESTEROL 12 [hp_X]/59.1mL - The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
    • CORTISONE ACETATE 18 [hp_X]/59.1mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
    • ESTRONE 18 [hp_X]/59.1mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
    • GAMBOGE 12 [hp_X]/59.1mL - A plant genus of the family CLUSIACEAE. Members contain XANTHONES.
    • KEROSENE 18 [hp_X]/59.1mL - A refined petroleum fraction used as a fuel as well as a solvent.
    • MILK THISTLE 4 [hp_X]/59.1mL
    • PARAFFIN 18 [hp_X]/59.1mL - A mixture of solid hydrocarbons obtained from petroleum. It has a wide range of uses including as a stiffening agent in ointments, as a lubricant, and as a topical anti-inflammatory. It is also commonly used as an embedding material in histology.
    • PHENACETIN 18 [hp_X]/59.1mL - A phenylacetamide that was formerly used in ANALGESICS but nephropathy and METHEMOGLOBINEMIA led to its withdrawal from the market. (From Smith and Reynard, Textbook of Pharmacology,1991, p431)
    • PHOSPHORUS 12 [hp_X]/59.1mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
    • PORK LIVER 9 [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.
    • SODIUM SULFATE 12 [hp_X]/59.1mL
    • TARAXACUM OFFICINALE 4 [hp_X]/59.1mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
    • THYROID, UNSPECIFIED 9 [hp_X]/59.1mL

    Which are Hepata-chord UNII Codes?

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

    Which are Hepata-chord Inactive Ingredients 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 for Hepata-chord?

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

    [5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".