43742-2221 NDC - METOX (ALLIUM SATIVUM, ARSENICUM ALBUM, ASCORBICUM ACIDUM, BERBERIS VULGARIS, BORON, CARBOLICUM ACIDUM, CYSTEINUM, FORMALINUM, GLYCYRRHIZA GLABRA, LANTHANUM METALLICUM, LAPPA MAJOR, L-METHIONINE, LYCOPODIUM CLAVATUM, MERCURIUS SOLUBILIS, NATRUM MURIATICUM, NIOBIUM METALLICUM, NUX VOMICA, PHYTOLACCA DECANDRA, PLUMBUM METALLICUM, STILLINGIA SYLVATICA, TANTALUM METALLICUM, THYROIDINUM (SUIS), TRIFOLIUM PRATENSE, ALUMINIUM METALLICUM, ANTIMONIUM CRUDUM, ARGENTUM METALLICUM, ARSENICUM ALBUM, AURUM METALLICUM,)

Drug Information

  • Product NDC: 43742-2221
  • Proprietary Name: Metox
  • Non Proprietary Name: Allium Sativum, Arsenicum Album, Ascorbicum Acidum, Berberis Vulgaris, Boron, Carbolicum Acidum, Cysteinum, Formalinum, Glycyrrhiza Glabra, Lanthanum Metallicum, Lappa Major, L-Methionine, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Niobium Metallicum, Nux Vomica, Phytolacca Decandra, Plumbum Metallicum, Stillingia Sylvatica, Tantalum Metallicum, Thyroidinum (Suis), Trifolium Pratense, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum,
  • Active Ingredient(s): 12 [hp_X]/mL ALUMINUM; 12 [hp_X]/mL ANTIMONY TRISULFIDE; 3 [hp_X]/mL ARCTIUM LAPPA ROOT; 1000 [hp_X]/mL ARSENIC TRIOXIDE; 6 [hp_X]/mL ASCORBIC ACID; 12 [hp_X]/mL BARIUM CARBONATE; 3 [hp_X]/mL BERBERIS VULGARIS ROOT BARK; 12 [hp_X]/mL BERYLLIUM; 12 [hp_X]/mL BISMUTH; 12 [hp_X]/mL BORON; 12 [hp_X]/mL BROMINE; 12 [hp_X]/mL CADMIUM; 12 [hp_X]/mL CERIUM; 12 [hp_X]/mL CESIUM CHLORIDE; 8 [hp_X]/mL CHROMIUM; 8 [hp_X]/mL COBALT; 8 [hp_X]/mL COPPER; 6 [hp_X]/mL CYSTEINE; 12 [hp_X]/mL DYSPROSIUM; 12 [hp_X]/mL ERBIUM; 12 [hp_X]/mL EUROPIUM; 12 [hp_X]/mL FORMALDEHYDE SOLUTION; 12 [hp_X]/mL GADOLINIUM; 3 [hp_X]/mL GARLIC; 12 [hp_X]/mL GERMANIUM SESQUIOXIDE; 3 [hp_X]/mL GLYCYRRHIZA GLABRA; 12 [hp_X]/mL GOLD; 12 [hp_X]/mL HOLMIUM; 12 [hp_X]/mL INDIUM; 8 [hp_X]/mL IODINE; 8 [hp_X]/mL IRIDIUM; 8 [hp_X]/mL IRON; 14 [hp_C]/mL LANTHANUM; 12 [hp_X]/mL LEAD; 8 [hp_X]/mL LITHIUM CARBONATE; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 8 [hp_X]/mL MAGNESIUM; 8 [hp_X]/mL MANGANESE; 12 [hp_X]/mL MERCURIUS SOLUBILIS; 8 [hp_X]/mL METHIONINE; 8 [hp_X]/mL MOLYBDENUM; 12 [hp_X]/mL NEODYMIUM OXIDE; 12 [hp_X]/mL NICKEL; 30 [hp_C]/mL NIOBIUM; 12 [hp_X]/mL OSMIUM; 12 [hp_X]/mL PALLADIUM; 12 [hp_X]/mL PHENOL; 8 [hp_X]/mL PHOSPHORUS; 8 [hp_X]/mL PHYTOLACCA AMERICANA ROOT; 12 [hp_X]/mL PLATINUM; 8 [hp_X]/mL POTASSIUM CARBONATE; 12 [hp_X]/mL PRASEODYMIUM; 12 [hp_X]/mL RHODIUM; 12 [hp_X]/mL RUBIDIUM; 12 [hp_X]/mL SAMARIUM; 8 [hp_X]/mL SELENIUM; 12 [hp_X]/mL SILVER; 8 [hp_X]/mL SODIUM CHLORIDE; 3 [hp_X]/mL STILLINGIA SYLVATICA ROOT; 8 [hp_X]/mL STRONTIUM CARBONATE; 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED; 8 [hp_X]/mL SULFUR; 30 [hp_C]/mL TANTALUM; 12 [hp_X]/mL TERBIUM; 12 [hp_X]/mL THALLIUM; 8 [hp_X]/mL THYROID; 12 [hp_X]/mL TIN; 8 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE; 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER; 15 [hp_C]/mL URANYL NITRATE HEXAHYDRATE; 8 [hp_X]/mL VANADIUM; 12 [hp_X]/mL YTTERBIUM OXIDE; 8 [hp_X]/mL ZINC
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Allergens [CS]; Ascorbic Acid [CS]; Blood Coagulation Factor [EPC]; Calcium [CS]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased IgG Production [PE]; Inhibit Ovum Fertilization [PE]; Mood Stabilizer [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Non-Standardized Plant Allergenic Extract [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Plant Proteins [CS]; Plant Proteins [CS]; Plant Proteins [CS]; Seed Storage Proteins [CS]; Standardized Chemical Allergen [EPC]; Standardized Chemical Allergen [EPC]; Standardized Chemical Allergen [EPC]; Standardized Chemical Allergen [EPC]; Vitamin C [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:1/17/2025

Package Information

No. Package Code Package Description Billing Unit
143742-2221-160 mL in 1 BOTTLE, DROPPER (43742-2221-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-2221The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEMetoxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAllium Sativum, Arsenicum Album, Ascorbicum Acidum, Berberis Vulgaris, Boron, Carbolicum Acidum, Cysteinum, Formalinum, Glycyrrhiza Glabra, Lanthanum Metallicum, Lappa Major, L-Methionine, Lycopodium Clavatum, Mercurius Solubilis, Natrum Muriaticum, Niobium Metallicum, Nux Vomica, Phytolacca Decandra, Plumbum Metallicum, Stillingia Sylvatica, Tantalum Metallicum, Thyroidinum (Suis), Trifolium Pratense, Aluminium Metallicum, Antimonium Crudum, Argentum Metallicum, Arsenicum Album, Aurum Metallicum,The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE1/17/2025This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALUMINUM; ANTIMONY TRISULFIDE; ARCTIUM LAPPA ROOT; ARSENIC TRIOXIDE; ASCORBIC ACID; BARIUM CARBONATE; BERBERIS VULGARIS ROOT BARK; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CERIUM; CESIUM CHLORIDE; CHROMIUM; COBALT; COPPER; CYSTEINE; DYSPROSIUM; ERBIUM; EUROPIUM; FORMALDEHYDE SOLUTION; GADOLINIUM; GARLIC; GERMANIUM SESQUIOXIDE; GLYCYRRHIZA GLABRA; GOLD; HOLMIUM; INDIUM; IODINE; IRIDIUM; IRON; LANTHANUM; LEAD; LITHIUM CARBONATE; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM; MANGANESE; MERCURIUS SOLUBILIS; METHIONINE; MOLYBDENUM; NEODYMIUM OXIDE; NICKEL; NIOBIUM; OSMIUM; PALLADIUM; PHENOL; PHOSPHORUS; PHYTOLACCA AMERICANA ROOT; PLATINUM; POTASSIUM CARBONATE; PRASEODYMIUM; RHODIUM; RUBIDIUM; SAMARIUM; SELENIUM; SILVER; SODIUM CHLORIDE; STILLINGIA SYLVATICA ROOT; STRONTIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; SULFUR; TANTALUM; TERBIUM; THALLIUM; THYROID; TIN; TRIBASIC CALCIUM PHOSPHATE; TRIFOLIUM PRATENSE FLOWER; URANYL NITRATE HEXAHYDRATE; VANADIUM; YTTERBIUM OXIDE; ZINCAn 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.
ACTIVE NUMERATOR STRENGTH12; 12; 3; 1000; 6; 12; 3; 12; 12; 12; 12; 12; 12; 12; 8; 8; 8; 6; 12; 12; 12; 12; 12; 3; 12; 3; 12; 12; 12; 8; 8; 8; 14; 12; 8; 12; 8; 8; 12; 8; 8; 12; 12; 30; 12; 12; 12; 8; 8; 12; 8; 12; 12; 12; 12; 8; 12; 8; 3; 8; 12; 8; 30; 12; 12; 8; 12; 8; 3; 15; 8; 12; 8 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Allergens [CS], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Dietary Proteins [CS], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Inhibit Ovum Fertilization [PE], Mood Stabilizer [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Plant Proteins [CS], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC], Vitamin C [EPC] 

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This page was last updated on: 4/4/2025

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