Metox

Allium Sativum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Phytolacca Decandra, Ascorbicum Acidum, Cysteinum, L-methionine, Thyroidinum (suis), Carbolicum Acidum, Formalinum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Carbolicum Acidum, Formalinum

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1220

Metox also known as Allium Sativum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Phytolacca Decandra, Ascorbicum Acidum, Cysteinum, L-methionine, Thyroidinum (suis), Carbolicum Acidum, Formalinum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Carbolicum Acidum, Formalinum is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Metox is 43742-1220. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Metox drug includes Aluminum - 12 [hp_X]/mL Antimony Trisulfide - 12 [hp_X]/mL Arctium Lappa Root - 3 [hp_X]/mL Arsenic Trioxide - 12 [hp_X]/mL Ascorbic Acid - 6 [hp_X]/mL Barium Carbonate - 12 [hp_X]/mL Berberis Vulgaris Root Bark - 3 [hp_X]/mL Beryllium - 12 [hp_X]/mL Bismuth - 12 [hp_X]/mL Boron - 12 [hp_X]/mL and more. The currest status of Metox drug is Active.

Drug Information:

Drug NDC:	43742-1220
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:	Metox
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 Sativum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Phytolacca Decandra, Ascorbicum Acidum, Cysteinum, L-methionine, Thyroidinum (suis), Carbolicum Acidum, Formalinum, Lycopodium Clavatum, Natrum Muriaticum, Nux Vomica, Aluminum Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum, Baryta Carbonica, Beryllium Metallicum, Bismuthum Metallicum, Boron, Bromium, Cadmium Metallicum, Carbolicum Acidum, Formalinum
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
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:	ALUMINUM - 12 [hp_X]/mL ANTIMONY TRISULFIDE - 12 [hp_X]/mL ARCTIUM LAPPA ROOT - 3 [hp_X]/mL ARSENIC TRIOXIDE - 12 [hp_X]/mL ASCORBIC ACID - 6 [hp_X]/mL BARIUM CARBONATE - 12 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 3 [hp_X]/mL BERYLLIUM - 12 [hp_X]/mL BISMUTH - 12 [hp_X]/mL BORON - 12 [hp_X]/mL Load more... BROMINE - 12 [hp_X]/mL CADMIUM - 12 [hp_X]/mL CERIUM - 12 [hp_X]/mL CESIUM CHLORIDE - 12 [hp_X]/mL CHROMIUM - 8 [hp_X]/mL COBALT - 8 [hp_X]/mL COPPER - 8 [hp_X]/mL CYSTEINE - 6 [hp_X]/mL DYSPROSIUM - 12 [hp_X]/mL ERBIUM - 12 [hp_X]/mL EUROPIUM - 12 [hp_X]/mL FORMALDEHYDE - 12 [hp_X]/mL GADOLINIUM - 12 [hp_X]/mL GARLIC - 3 [hp_X]/mL GERMANIUM SESQUIOXIDE - 12 [hp_X]/mL GLYCYRRHIZA GLABRA - 3 [hp_X]/mL GOLD - 12 [hp_X]/mL HOLMIUM - 12 [hp_X]/mL INDIUM - 12 [hp_X]/mL IODINE - 8 [hp_X]/mL IRIDIUM - 8 [hp_X]/mL IRON - 8 [hp_X]/mL LANTHANUM - 14 [hp_C]/mL LEAD - 12 [hp_X]/mL LITHIUM CARBONATE - 8 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/mL MAGNESIUM - 8 [hp_X]/mL MANGANESE - 8 [hp_X]/mL MERCURIUS SOLUBILIS - 12 [hp_X]/mL METHIONINE - 8 [hp_X]/mL MOLYBDENUM - 8 [hp_X]/mL NEODYMIUM OXIDE - 12 [hp_X]/mL NICKEL - 12 [hp_X]/mL NIOBIUM - 30 [hp_C]/mL OSMIUM - 12 [hp_X]/mL PALLADIUM - 12 [hp_X]/mL PHENOL - 12 [hp_X]/mL PHOSPHORUS - 8 [hp_X]/mL PHYTOLACCA AMERICANA ROOT - 4 [hp_X]/mL PLATINUM - 12 [hp_X]/mL POTASSIUM CARBONATE - 8 [hp_X]/mL PRASEODYMIUM - 12 [hp_X]/mL RHODIUM - 12 [hp_X]/mL RUBIDIUM NITRITE - 12 [hp_X]/mL SAMARIUM - 12 [hp_X]/mL SELENIUM - 8 [hp_X]/mL SILVER - 12 [hp_X]/mL SODIUM CHLORIDE - 8 [hp_X]/mL STILLINGIA SYLVATICA ROOT - 3 [hp_X]/mL STRONTIUM CARBONATE - 8 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL SULFUR - 8 [hp_X]/mL SUS SCROFA THYROID - 8 [hp_X]/mL TANTALUM - 30 [hp_C]/mL TERBIUM - 12 [hp_X]/mL THALLIUM - 12 [hp_X]/mL TIN - 12 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE - 8 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 3 [hp_X]/mL URANYL NITRATE HEXAHYDRATE - 12 [hp_X]/mL VANADIUM - 8 [hp_X]/mL YTTERBIUM OXIDE - 12 [hp_X]/mL ZINC - 8 [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:	24 Apr, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	18 Jun, 2023
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:	05 May, 2026
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:	Deseret Biologicals, Inc.
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:	N0000193618 M0001797 N0000185508 N0000175629 N0000184306 M0000728 M0005152 N0000175831 N0000008595 N0000008924 N0000175830 N0000185371 M0006342 M0016962 N0000185375 N0000185001 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	CPD4NFA903 F79059A38U 597E9BI3Z3 S7V92P67HO PQ6CK8PD0R 6P669D8HQ8 1TH8Q20J0U OW5102UV6N U015TT5I8H N9E3X5056Q Load more... SBV4XY874G 00BH33GNGH 30K4522N6T GNR9HML8BA 0R0008Q3JB 3G0H8C9362 789U1901C5 K848JZ4886 1D4N45714Q 77B218D3YE 444W947O8O 1HG84L3525 AU0V1LM3JT V1V998DC17 96WE91N25T 2788Z9758H 79Y1949PYO W1XX32SQN1 045A6V3VFX 9679TC07X4 44448S9773 E1UOL152H7 6I3K30563S 2P299V784P 2BMD2GNA4V C88X29Y479 I38ZP9992A 42Z2K6ZL8P 324Y4038G2 AE28F7PNPL 81AH48963U AYT3H319PN 7OV03QG267 05175J654G 2E7M255OPY 5TWQ1V240M 339NCG44TV 27YLU75U4W 11E6VI8VEG 49DFR088MY BQN1B9B9HA NKN7EZA750 DMK383DSAC 93722E7JA1 42OD65L39F H6241UJ22B 3M4G523W1G 451W47IQ8X QBR70R4FBK 41YPU4MMCA 269XH13919 70FD1KFU70 6RV024OAUQ 6424HBN274 06SSF7P179 AD84R52XLF 387GMG9FH5 91D9GV0Z28 4JS0838828 3V057702FY 00J9J9XKDE T66CZ53RP4 J41CSQ7QDS
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:	Vitamin C [EPC] Standardized Chemical Allergen [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:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Inhibit Ovum Fertilization [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:	Ascorbic Acid [CS] Allergens [CS] Copper [CS] Dietary Proteins [CS] Plant 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] Ascorbic Acid [CS] Blood Coagulation Factor [EPC] Calcium [CS] Cations Divalent [CS] Cell-mediated Immunity [PE] Copper [CS] Copper-containing Intrauterine Device [EPC] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Dietary Proteins [CS] Increased Coagulation Factor Activity [PE] Increased Histamine Release [PE] Increased IgG Production [PE] Inhibit Ovum Fertilization [PE] Mood Stabilizer [EPC] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Seed Storage Proteins [CS] Standardized Chemical Allergen [EPC] Vitamin C [EPC]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1220-1	30 mL in 1 BOTTLE, DROPPER (43742-1220-1)	24 Apr, 2018	18 Jun, 2023	No
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.

Other medicines with the same generic name

Metox

Allium Sativum & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1220

Purpose:

Homeopathic indications: for temporary relief of symptoms related to heavy metal toxicity including cough, poor concentration, nausea, vomiting, occasional diarrhea, stomach pain, headache, sweating, and a metallic taste in the mouth.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Metox allium sativum, berberis vulgaris, glycyrrhiza glabra, lappa major, stillingia sylvatica, trifolium pratense, phytolacca decandra, ascorbicum acidum, cysteinum, l-methionine, thyroidinum (suis), carbolicum acidum, formalinum, lycopodium clavatum, natrum muriaticum, nux vomica, aluminum metallicum, antimonium crudum, argentum metallicum, arsenicum album, aurum metallicum, baryta carbonica, beryllium metallicum, bismuthum metallicum, boron, bromium, cadmium metallicum, carbolicum acidum, formalinum garlic garlic berberis vulgaris root bark berberis vulgaris root bark glycyrrhiza glabra glycyrrhiza glabra arctium lappa root arctium lappa root stillingia sylvatica root stillingia sylvatica root trifolium pratense flower trifolium pratense flower phytolacca americana root phytolacca americana root ascorbic acid ascorbic acid cysteine cysteine methionine methionine sus scrofa thyroid sus scrofa thyroid tribasic calcium phosphate calcium cation chromium chromium cobalt cobalt copper copper iron iron iodine iodine iridium iridium potassium carbonate carbonate ion lithium carbonate lithium cation magnesium magnesium manganese manganese molybdenum molybdenum sodium chloride chloride ion phosphorus phosphorus selenium selenium strontium carbonate strontium cation sulfur sulfur vanadium vanadium zinc zinc phenol phenol formaldehyde formaldehyde lycopodium clavatum spore lycopodium clavatum spore strychnos nux-vomica seed strychnos nux-vomica seed boron boron aluminum aluminum antimony trisulfide antimony trisulfide silver silver arsenic trioxide arsenic cation (3+) gold gold barium carbonate barium cation beryllium beryllium bismuth bismuth bromine bromine cadmium cadmium cerium cerium cesium chloride cesium cation dysprosium dysprosium erbium erbium europium europium gadolinium gadolinium germanium sesquioxide germanium sesquioxide holmium holmium indium indium mercurius solubilis mercurius solubilis neodymium oxide neodymium oxide nickel nickel osmium osmium palladium palladium platinum platinum lead lead praseodymium praseodymium rhodium rhodium rubidium nitrite rubidium cation nitrite ion samarium samarium tin tin terbium terbium thallium thallium uranyl nitrate hexahydrate uranium cation (6+) ytterbium oxide ytterbium oxide lanthanum lanthanum niobium niobium tantalum tantalum water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact a physician or poison control center right away. if pregnant or breast-feeding, seek advice of a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing.

Dosage and Administration:

Directions: 1-10 drops under the tongue, 3 times a day or as directed by a health professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1220-1 homeopathic metox 1 fl oz (30 ml) metox

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com **for a complete list of heavy metal isodes ii and heavy metal isodes contact deseret biologicals, inc.

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.