62185-0034 NDC - METDETOX (ALLIUM SATIVUM, BERBERIS VULGARIS, GLYCYRRHIZA GLABRA, LAPPA MAJOR, STILLINGIA SYLVATICA, TRIFOLIUM PRATENSE, ASCORBICUM ACIDUM, CYSTEINUM, L-METHIONINE, PHYTOLACCA DECANDRA, THYROIDINUM (SUIS), CALCAREA PHOSPHORICA, CHROMIUM METALLICUM, COBALTUM METALLICUM, CUPRUM METALLICUM, FERRUM METALLICUM, IODIUM, IRIDIUM METALLICUM, KALI CARBONICUM, LITHIUM CARBONICUM, MAGNESIUM METALLICUM, MANGANUM METALLICUM, MOLYBDENUM, NATRUM MURIATICUM, PHOSPHORUS, SELENIUM METALLICUM, STRONTIUM CARBONICUM, SULPHUR)

Drug Information

  • Product NDC: 62185-0034
  • Proprietary Name: MetDetox
  • Non Proprietary Name: Allium Sativum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Ascorbicum Acidum, Cysteinum, L-Methionine, Phytolacca Decandra, Thyroidinum (Suis), Calcarea Phosphorica, Chromium Metallicum, Cobaltum Metallicum, Cuprum Metallicum, Ferrum Metallicum, Iodium, Iridium Metallicum, Kali Carbonicum, Lithium Carbonicum, Magnesium Metallicum, Manganum Metallicum, Molybdenum, Natrum Muriaticum, Phosphorus, Selenium Metallicum, Strontium Carbonicum, Sulphur
  • Active Ingredient(s): 12 [hp_X]/mL ALUMINUM; 12 [hp_X]/mL ANTIMONY TRISULFIDE; 3 [hp_X]/mL ARCTIUM LAPPA ROOT; 3 [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; 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; 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 NITRITE; 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; 8 [hp_X]/mL SUS SCROFA THYROID; 30 [hp_C]/mL TANTALUM; 12 [hp_X]/mL TERBIUM; 12 [hp_X]/mL THALLIUM; 12 [hp_X]/mL TIN; 8 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE; 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER; 12 [hp_X]/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]; 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]; 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 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]; Standardized Chemical Allergen [EPC]; Vitamin C [EPC]

Labeler Information

Field Name Field Value
Labeler Name: Dr. Donna Restivo DC
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:7/31/2018
End Marketing Date:1/11/2026

Package Information

No. Package Code Package Description Billing Unit
162185-0034-130 mL in 1 BOTTLE, DROPPER (62185-0034-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC62185-0034The 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 NAMEMetDetoxThe 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, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Ascorbicum Acidum, Cysteinum, L-Methionine, Phytolacca Decandra, Thyroidinum (Suis), Calcarea Phosphorica, Chromium Metallicum, Cobaltum Metallicum, Cuprum Metallicum, Ferrum Metallicum, Iodium, Iridium Metallicum, Kali Carbonicum, Lithium Carbonicum, Magnesium Metallicum, Manganum Metallicum, Molybdenum, Natrum Muriaticum, Phosphorus, Selenium Metallicum, Strontium Carbonicum, SulphurThe 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 DATE7/31/2018This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE1/11/2026This 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.
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 NAMEDr. Donna Restivo DCName of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEALUMINUM; ANTIMONY TRISULFIDE; ARCTIUM LAPPA ROOT; ASCORBIC ACID; BARIUM CARBONATE; BERBERIS VULGARIS ROOT BARK; BERYLLIUM; BISMUTH; BORON; BROMINE; CADMIUM; CERIUM; CESIUM; CHROMIUM; COBALT; COPPER; CYSTEINE; DYSPROSIUM; ERBIUM; EUROPIUM; FORMALDEHYDE; 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 NITRITE; SAMARIUM; SELENIUM; SILVER; SODIUM CHLORIDE; STILLINGIA SYLVATICA ROOT; STRONTIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; SULFUR; SUS SCROFA THYROID; TANTALUM; TERBIUM; THALLIUM; 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; 3; 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; 8; 30; 12; 12; 12; 8; 3; 12; 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_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_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 
PHARM CLASSESAllergens [CS], 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], 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 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], Standardized Chemical Allergen [EPC], Vitamin C [EPC] 

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This page was last updated on: 11/21/2025

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