NDC 64578-0131 Bacteria Chord

Azadirachta Indica,Belladonna,Berberis Vulgaris,Boldo,Candida Albicans,Ceanothus - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
64578-0131
Proprietary Name:
Bacteria Chord
Non-Proprietary Name: [1]
Azadirachta Indica, Belladonna, Berberis Vulgaris, Boldo, Candida Albicans, Ceanothus Americanus, Cetraria Islandica, Crotalus Horridus, Echinacea (angustifolia), Glandula Suprarenalis Suis, Glycyrrhiza Glabra, Hamamelis Virginiana, Hepar Suis, Hydrastis Canadensis, Hydrocotyle Asiatica, Hypericum Perforatum, Lappa Major, Ledum Palustre, Millefolium, Morbillinum, Myrrha, Pancreas Suis, Pertussinum, Phosphorus, Plantago Major, Pyrogenium, Solidago Virgaurea, Zingiber Officinale
Substance Name: [2]
Achillea Millefolium; Arctium Lappa Root; Atropa Belladonna; Azadirachta Indica Bark; Berberis Vulgaris Root Bark; Candida Albicans; Ceanothus Americanus Leaf; Centella Asiatica; Cetraria Islandica Subsp. Islandica; Crotalus Horridus Horridus Venom; Echinacea Angustifolia; Ginger; Glycyrrhiza Glabra; Goldenseal; Hamamelis Virginiana Root Bark/stem Bark; Human Sputum, Bordetella Pertussis Infected; Hypericum Perforatum; Ledum Palustre Twig; Measles Virus; Myrrh; Peumus Boldus Leaf; Phosphorus; Plantago Major; Pork Liver; Rancid Beef; Solidago Virgaurea Flowering Top; Sus Scrofa Adrenal Gland; Sus Scrofa Pancreas
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]
    11-11-2016
    Listing Expiration Date: [11]
    12-31-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 64578-0131-1

    Package Description: 59 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 64578-0131?

    The NDC code 64578-0131 is assigned by the FDA to the product Bacteria Chord which is a human over the counter drug product labeled by Energetix Corp. The generic name of Bacteria Chord is azadirachta indica, belladonna, berberis vulgaris, boldo, candida albicans, ceanothus americanus, cetraria islandica, crotalus horridus, echinacea (angustifolia), glandula suprarenalis suis, glycyrrhiza glabra, hamamelis virginiana, hepar suis, hydrastis canadensis, hydrocotyle asiatica, hypericum perforatum, lappa major, ledum palustre, millefolium, morbillinum, myrrha, pancreas suis, pertussinum, phosphorus, plantago major, pyrogenium, solidago virgaurea, zingiber officinale. 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 64578-0131-1 59 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 Bacteria 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 Bacteria 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 Bacteria Chord UNII Codes?

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

    Which are Bacteria 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 Bacteria 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".