NDC 61062-0007 Metdetox

Allium Sativum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Stillingia Sylvatica, Trifolium Pratense, Ascorbic Acid,

NDC Product Code 61062-0007

NDC Code: 61062-0007

Proprietary Name: Metdetox What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Allium Sativum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Stillingia Sylvatica, Trifolium Pratense, Ascorbic Acid, 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.

NDC Code Structure

  • 61062 - Restivo Chiropractic
    • 61062-0007 - Metdetox

NDC 61062-0007-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Metdetox with NDC 61062-0007 is a a human over the counter drug product labeled by Restivo Chiropractic. The generic name of Metdetox is allium sativum, berberis vulgaris, glycyrrhiza glabra, lappa major, phytolacca decandra, stillingia sylvatica, trifolium pratense, ascorbic acid,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Restivo Chiropractic

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.

Product Type: Human Otc Drug 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.

Metdetox Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • GARLIC 3 [hp_X]/mL
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • ASCORBIC ACID 6 [hp_X]/mL
  • CYSTEINE 6 [hp_X]/mL
  • IRIDIUM 8 [hp_X]/mL
  • METHIONINE 8 [hp_X]/mL
  • SELENIUM 8 [hp_X]/mL
  • THYROID, PORCINE 8 [hp_X]/mL
  • ARSENIC TRIOXIDE 12 [hp_X]/mL
  • PHENOL 12 [hp_X]/mL
  • FORMALDEHYDE 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • SODIUM CHLORIDE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • ANTIMONY TRISULFIDE 12 [hp_X]/mL
  • ALUMINUM 12 [hp_X]/mL
  • SILVER 12 [hp_X]/mL
  • GOLD 12 [hp_X]/mL
  • BARIUM CARBONATE 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 12 [hp_X]/mL
  • CHROMIUM 12 [hp_X]/mL
  • COBALT 12 [hp_X]/mL
  • COPPER 12 [hp_X]/mL
  • DYSPROSIUM 12 [hp_X]/mL
  • ERBIUM 12 [hp_X]/mL
  • EUROPIUM OXIDE 112 [hp_X]/mL
  • IRON 12 [hp_X]/mL
  • GADOLINIUM OXIDE 12 [hp_X]/mL
  • GERMANIUM SESQUIOXIDE 12 [hp_X]/mL
  • HOLMIUM 12 [hp_X]/mL
  • LANTHANUM OXIDE 12 [hp_X]/mL
  • LITHIUM CARBONATE 12 [hp_X]/mL
  • MAGNESIUM 12 [hp_X]/mL
  • MANGANESE 12 [hp_X]/mL
  • MERCURIUS SOLUBILIS 12 [hp_X]/mL
  • MOLYBDENUM 12 [hp_X]/mL
  • NEODYMIUM OXIDE 12 [hp_X]/mL
  • NICKEL 12 [hp_X]/mL
  • NIOBIUM 12 [hp_X]/mL
  • OSMIUM 12 [hp_X]/mL
  • PALLADIUM 12 [hp_X]/mL
  • PLATINUM 12 [hp_X]/mL
  • LEAD 12 [hp_X]/mL
  • PRASEODYMIUM 12 [hp_X]/mL
  • RHODIUM 12 [hp_X]/mL
  • RUBIDIUM 12 [hp_X]/mL
  • SAMARIUM OXIDE 12 [hp_X]/mL
  • TIN 12 [hp_X]/mL
  • STRONTIUM CARBONATE 12 [hp_X]/mL
  • TANTALUM 12 [hp_X]/mL
  • TERBIUM 12 [hp_X]/mL
  • THALLIUM 12 [hp_X]/mL
  • URANYL NITRATE HEXAHYDRATE 12 [hp_X]/mL
  • VANADIUM 12 [hp_X]/mL
  • YTTERBIUM OXIDE 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Restivo Chiropractic
Labeler Code: 61062
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 12-10-2013 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 07-01-2019 What is the End Marketing Date?
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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Metdetox Product Label Images

Metdetox Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Allium sativum 3X, Berberis vulgaris 3X, Glycyrrhiza glabra 3X, Lappa major 3X, Phytolacca decandra 3X, Stillingia sylvatica 3X, Trifolium pratense 3X, Ascorbic acid 6X, Cysteinum 6X, Iridium metallicum 8X, Methionine 8X, Selenium metallicum 8X, Thyroidinum (suis) 8X, Arsenicum album 12X, Carbolicum acidum 12X, Formalinum 12X, Lycopodium clavatum 12X, Natrum muriaticum 12X, Nux vomica 12X, Antimonium crudum 12X, Aluminum metallicum 12X, 30X, Argentum metallicum 12X, 30X, Aurum metallicum 12X, 30X, Baryta carbonica 2X, 30X, Beryllium metallicum 12X, 30X, Bismuthum metallicum 12X, 30X, Boron 12X, 30X, Bromium 12X, 30X, Cadmium metallicum 12X, 30X, Cerium 12X, 30X, Cesium chloride 12X, 30X, Chromium 12X, 30X, Cobaltum metallicum 12X, 30X, Cuprum metallicum 12X, 30X, Dysprosium 12X, 30X, Erbium 12X, 30X, Europium oxide 12X, 30X, Ferrum metallicum 12X, 30X, Gadolinium oxide 12X, 30X, Germanium sesquioxide 12X, 30X, Holmium 12X, 30X, Iridium metallicum 12X, 30X, Lanthanum oxide 12X, 30X, Lithium carbonicum 12X, 30X, Magnesium metallicum 12X, 30X, Manganum metallicum 12X, 30X, Mercurius solubilis 12X, 30X, Molybdenum 12X, 30X, Neodymium oxide 12X, 30X, Niccolum metallicum 12X, 30X, Niobium 12X, 30X, Osmium metallicum 12X, 30X, Palladium metallicum 12X, 30X, Platinum metallicum 12X, 30X, Plumbum metallicum 12X, 30X, Praseodymium 12X, 30X, Rhodium metallicum 12X, 30X, Rubidium 12X, 30X, Samarium oxide 12X, 30X, Selenium metallicum 12X, 30X, Stannum metallicum 12X, 30X, Strontium carbonicum 12X, 30X, Tantalum 12X, 30X, Terbium 12X, 30X, Thallium metallicum 12X, 30X, Uranium nitricum 12X, 30X, Vanadium metallicum 12X, 30X, Ytterbium oxide 12X, 30X, Zincum metallicum 12X, 30X.

Indications:

For temporary relief of symptoms related to heavy metal toxicity including gastritis, cough, poor concentration, nausea, vomiting, diarrhea, stomach pain, headache, sweating, and a metallic taste in the mouth.

For temporary relief of symptoms related to heavy metal toxicity including gastritis, cough, poor concentration, nausea, vomiting, diarrhea, stomach pain, headache, sweating, and a metallic taste in the mouth.

Warnings:

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper Seal:  Sealed for your protection.  Do not use if seal is broken or missing.

Keep Out Of Reach Of Children.

Keep out of reach of children.  In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops under the tongue, 3 to 6 times per day or as directed by a health professional.  Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized water, 25% Ethanol.

Questions:

Distributed by: Restivo Chiropractic822 South Lake Blvd, Mahopac, New York 10541www.mahopacmassage.com

Package Label Display:

NDC 61062-0007-1HOMEOPATHICMetDETOX1 FL OZ (30 ml)

* Please review the disclaimer below.

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