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NDC 64578-0132 Tox-chord

Alfalfa,Alumina,Benzoicum Acidum,Carboneum,Cetraria Islandica,Folliculinum,Fucus - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 64578-0132?
  4. Tox-chord Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
64578-0132
Proprietary Name:
Tox-chord
Non-Proprietary Name: [1]
Alfalfa, Alumina, Benzoicum Acidum, Carboneum, Cetraria Islandica, Folliculinum, Fucus Vesiculosus, Fumaricum Acidum, Hepar Suis, Kali Carbonicum, Kreosotum, Natrum Muriaticum, Paraffinum, Petroleum, Phosphoricum Acidum, Phosphorus, Pix Liquida, Plantago Major, Plumbum Metallicum, Pulsatilla (vulgaris), Radium Bromatum, Resorcinum, Salol, Silicea, Symphytum Officinale, Tabacum, Terebinthina, Thyroidinum (bovine), Triticum Repens, Zincum Oxydatum
Substance Name: [2]
Alfalfa; Aluminum Oxide; Benzoic Acid; Cetraria Islandica Subsp. Islandica; Comfrey Root; D&c Black No. 2; Elymus Repens Root; Estrone; Fucus Vesiculosus; Fumaric Acid; Kerosene; Lead; Paraffin; Phenyl Salicylate; Phosphoric Acid; Phosphorus; Pine Tar; Plantago Major; Pork Liver; Potassium Carbonate; Pulsatilla Vulgaris; Radium Bromide; Resorcinol; Silicon Dioxide; Sodium Chloride; Thyroid, Bovine; Tobacco Leaf; Turpentine Oil; Wood Creosote; Zinc Oxide
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
    Product Label ID:
    6b0d1628-b20d-426e-9c84-5cceadca3f45
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    11-11-2016
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 64578-0132-1

    Package Description: 59.1 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 64578-0132?

    The NDC code 64578-0132 is assigned by the FDA to the product Tox-chord which is a human over the counter drug product labeled by Energetix Corp. The generic name of Tox-chord is alfalfa, alumina, benzoicum acidum, carboneum, cetraria islandica, folliculinum, fucus vesiculosus, fumaricum acidum, hepar suis, kali carbonicum, kreosotum, natrum muriaticum, paraffinum, petroleum, phosphoricum acidum, phosphorus, pix liquida, plantago major, plumbum metallicum, pulsatilla (vulgaris), radium bromatum, resorcinum, salol, silicea, symphytum officinale, tabacum, terebinthina, thyroidinum (bovine), triticum repens, zincum oxydatum. 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 64578-0132-1 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 the uses for Tox-chord?

    Take 30 drops orally twice daily or as directed by a healthcare professional.Consult a physician for use in children under 12 years of age or if symptoms worsen or persist.

    What are Tox-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.

    Which are Tox-chord UNII Codes?

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

    Which are Tox-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 Tox-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".