Metal-chord

Allium Cepa, Allium Sativum, Alpha-lipoicum Acidum, Alumina, Arsenicum Metallicum, Berberis Vulgaris, Cadmium Metallicum, Carduus Marianus, Cetraria Islandica, Cuprum Metallicum, Cysteinum, Glycyrrhiza Glabra, Hepar Suis, Lappa Major, Lycopodium Clavatum, Mercurius Solubilis, Nux Vomica, Plantago Major, Plumbum Metallicum, Pyridoxinum Hydrochloricum, Selenium Metallicum, Stillingia Sylvatica, Thyroidinum, Trifolium Pratense, Zingiber Officinale


Energetix Corp
Human Otc Drug
NDC 64578-0068
Metal-chord also known as Allium Cepa, Allium Sativum, Alpha-lipoicum Acidum, Alumina, Arsenicum Metallicum, Berberis Vulgaris, Cadmium Metallicum, Carduus Marianus, Cetraria Islandica, Cuprum Metallicum, Cysteinum, Glycyrrhiza Glabra, Hepar Suis, Lappa Major, Lycopodium Clavatum, Mercurius Solubilis, Nux Vomica, Plantago Major, Plumbum Metallicum, Pyridoxinum Hydrochloricum, Selenium Metallicum, Stillingia Sylvatica, Thyroidinum, Trifolium Pratense, Zingiber Officinale is a human otc drug labeled by 'Energetix Corp'. National Drug Code (NDC) number for Metal-chord is 64578-0068. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Metal-chord drug includes .alpha.-lipoic Acid - 12 [hp_X]/mL Aluminum Oxide - 15 [hp_X]/mL Arctium Lappa Root - 4 [hp_X]/mL Arsenic - 15 [hp_X]/mL Berberis Vulgaris Root Bark - 4 [hp_X]/mL Cadmium - 15 [hp_X]/mL Cetraria Islandica Subsp. Islandica - 12 [hp_X]/mL Copper - 15 [hp_X]/mL Cysteine - 12 [hp_X]/mL Garlic - 6 [hp_X]/mL and more. The currest status of Metal-chord drug is Active.

Drug Information:

Drug NDC: 64578-0068
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name: Metal-chord
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type: Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name: Allium Cepa, Allium Sativum, Alpha-lipoicum Acidum, Alumina, Arsenicum Metallicum, Berberis Vulgaris, Cadmium Metallicum, Carduus Marianus, Cetraria Islandica, Cuprum Metallicum, Cysteinum, Glycyrrhiza Glabra, Hepar Suis, Lappa Major, Lycopodium Clavatum, Mercurius Solubilis, Nux Vomica, Plantago Major, Plumbum Metallicum, Pyridoxinum Hydrochloricum, Selenium Metallicum, Stillingia Sylvatica, Thyroidinum, Trifolium Pratense, Zingiber Officinale
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name: Energetix Corp
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form: Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status: Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:.ALPHA.-LIPOIC ACID - 12 [hp_X]/mL
ALUMINUM OXIDE - 15 [hp_X]/mL
ARCTIUM LAPPA ROOT - 4 [hp_X]/mL
ARSENIC - 15 [hp_X]/mL
BERBERIS VULGARIS ROOT BARK - 4 [hp_X]/mL
CADMIUM - 15 [hp_X]/mL
CETRARIA ISLANDICA SUBSP. ISLANDICA - 12 [hp_X]/mL
COPPER - 15 [hp_X]/mL
CYSTEINE - 12 [hp_X]/mL
GARLIC - 6 [hp_X]/mL
GINGER - 6 [hp_X]/mL
GLYCYRRHIZA GLABRA - 4 [hp_X]/mL
LEAD - 15 [hp_X]/mL
LYCOPODIUM CLAVATUM SPORE - 4 [hp_X]/mL
MERCURIUS SOLUBILIS - 15 [hp_X]/mL
MILK THISTLE - 4 [hp_X]/mL
ONION - 6 [hp_X]/mL
PLANTAGO MAJOR - 4 [hp_X]/mL
PORK LIVER - 9 [hp_X]/mL
PYRIDOXINE HYDROCHLORIDE - 12 [hp_X]/mL
SELENIUM - 15 [hp_X]/mL
STILLINGIA SYLVATICA ROOT - 4 [hp_X]/mL
STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL
THYROID, BOVINE - 9 [hp_X]/mL
TRIFOLIUM PRATENSE FLOWER - 4 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Marketing Category: UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date: 20 Jun, 2014
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date: 13 Jun, 2026
This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
Listing Expiration Date: 31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.
Manufacturer Name:Energetix Corp
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:Yes
Whether or not the drug has been repackaged for distribution.
NUI:M0005152
N0000175831
N0000008595
N0000008924
N0000175830
N0000185371
N0000175629
N0000184306
M0000728
M0006342
M0016962
N0000185375
M0008672
M0022575
N0000185001
M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:73Y7P0K73Y
LMI26O6933
597E9BI3Z3
N712M78A8G
1TH8Q20J0U
00BH33GNGH
BJ7YPN79A1
789U1901C5
K848JZ4886
V1V998DC17
C5529G5JPQ
2788Z9758H
2P299V784P
C88X29Y479
324Y4038G2
U946SH95EE
492225Q21H
W2469WNO6U
6EC706HI7F
68Y4CF58BV
H6241UJ22B
QBR70R4FBK
269XH13919
MN18OTN73W
4JS0838828
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:Copper-containing Intrauterine Device [EPC]
Non-Standardized Food Allergenic Extract [EPC]
Non-Standardized Plant Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:Decreased Embryonic Implantation [PE]
Decreased Sperm Motility [PE]
Inhibit Ovum Fertilization [PE]
Increased Histamine Release [PE]
Cell-mediated Immunity [PE]
Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:Copper [CS]
Allergens [CS]
Dietary Proteins [CS]
Plant Proteins [CS]
Food Additives [CS]
Vegetable Proteins [CS]
Seed Storage Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:Allergens [CS]
Analogs/Derivatives [Chemical/Ingredient]
Cell-mediated Immunity [PE]
Copper [CS]
Copper-containing Intrauterine Device [EPC]
Decreased Embryonic Implantation [PE]
Decreased Sperm Motility [PE]
Dietary Proteins [CS]
Food Additives [CS]
Increased Histamine Release [PE]
Increased IgG Production [PE]
Inhibit Ovum Fertilization [PE]
Non-Standardized Food Allergenic Extract [EPC]
Non-Standardized Plant Allergenic Extract [EPC]
Plant Proteins [CS]
Seed Storage Proteins [CS]
Vegetable Proteins [CS]
Vitamin B 6 [Chemical/Ingredient]
Vitamin B6 Analog [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
64578-0068-159.1 mL in 1 BOTTLE, DROPPER (64578-0068-1)30 May, 2017N/ANo
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Purpose:

Purpose temporary relief of metallic taste, irritability, difficulty concentrating.

Product Elements:

Metal-chord allium cepa, allium sativum, alpha-lipoicum acidum, alumina, arsenicum metallicum, berberis vulgaris, cadmium metallicum, carduus marianus, cetraria islandica, cuprum metallicum, cysteinum, glycyrrhiza glabra, hepar suis, lappa major, lycopodium clavatum, mercurius solubilis, nux vomica, plantago major, plumbum metallicum, pyridoxinum hydrochloricum, selenium metallicum, stillingia sylvatica, thyroidinum, trifolium pratense, zingiber officinale onion onion garlic garlic .alpha.-lipoic acid .alpha.-lipoic acid aluminum oxide aluminum oxide arsenic arsenic berberis vulgaris root bark berberis vulgaris root bark cadmium cadmium milk thistle milk thistle cetraria islandica subsp. islandica cetraria islandica subsp. islandica copper copper cysteine cysteine glycyrrhiza glabra glycyrrhiza glabra pork liver pork liver arctium lappa root arctium lappa root lycopodium clavatum spore lycopodium clavatum spore mercurius solubilis mercurius solubilis strychnos nux-vomica seed strychnos nux-vomica seed plantago major plantago major lead lead pyridoxine hydrochloride pyridoxine selenium selenium stillingia sylvatica root stillingia sylvatica root thyroid, bovine thyroid, bovine trifolium pratense flower trifolium pratense flower ginger ginger water glycerin alcohol

Indications and Usage:

Uses temporary relief of metallic taste, irritability, difficulty concentrating.

Warnings:

Warnings in case of overdose, get medical help or call a poison control center right away. if pregnant or breast-feeding, ask a health professional before use. keep out of reach of children.

Dosage and Administration:

Directions take 5 drops orally once daily, working up to 30 drops 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.

Package Label Principal Display Panel:

Energetix metal-chord homeopathic remedy metallic taste, irritability, difficulty concentrating 2 fl oz (59.1 ml) purpose temporary relief of metallic taste, irritability, difficulty concentrating. 2oz bottle label

Further Questions:

Distributed by energetix corp dahlonega, ga 30533 questions? 800.990.7085


Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.