Heavy Metal-amalga Detox Liquid
NDC 55714-4805

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 55714-4805?
  4. Heavy Metal-amalga Detox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Heavy Metal-amalga Detox (allium sativum, aluminium metallicum, arg. met., aur. met., baryta carb., beryllium metallicum, bismuthum metallicum, cadmium metallicum, calc. fluor., carbo veg., chelidonium majus, cinchona, cobaltum met., cuprum met., glycyrrhiza glabra, hydrofluoricum acidum, iris versicolor, manganum metallicum, merc. viv., niccolum metallicum, osmium metallicum, platinum met., plumb. met., stannum met., strontium carb., thallium metallicum, titanium metallicum, carduus mar., taraxacum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Newton Laboratories, Inc.. This medication is typically used as a allergens [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 55714-4805 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
55714-4805
Proprietary Name:
Heavy Metal-amalga Detox
Non-Proprietary Name: [1]
Allium Sativum, Aluminium Metallicum, Arg. Met., Aur. Met., Baryta Carb., Beryllium Metallicum, Bismuthum Metallicum, Cadmium Metallicum, Calc. Fluor., Carbo Veg., Chelidonium Majus, Cinchona, Cobaltum Met., Cuprum Met., Glycyrrhiza Glabra, Hydrofluoricum Acidum, Iris Versicolor, Manganum Metallicum, Merc. Viv., Niccolum Metallicum, Osmium Metallicum, Platinum Met., Plumb. Met., Stannum Met., Strontium Carb., Thallium Metallicum, Titanium Metallicum, Carduus Mar., Taraxacum
Substance Name: [2]
Activated Charcoal; Aluminum; Barium Carbonate; Beryllium; Bismuth; Cadmium; Calcium Fluoride; Chelidonium Majus; Cinchona Officinalis Bark; Cobalt; Copper; Garlic; Glycyrrhiza Glabra; Gold; Hydrofluoric Acid; Iris Versicolor Root; Lead; Manganese; Mercury; Milk Thistle; Nickel; Osmium; Platinum; Silver Nitrate; Strontium Carbonate; Taraxacum Officinale; Thallium; Tin; Titanium
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

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.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Newton Laboratories, Inc.
Labeler Code:
55714
Product Label ID:
99d7d83b-85f8-a4bf-e053-2995a90a703f
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
09-02-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 55714-4805?

The NDC code 55714-4805 is assigned by the FDA to the product Heavy Metal-amalga Detox. It is commonly known by its generic name, allium sativum, aluminium metallicum, arg. met., aur. met., baryta carb., beryllium metallicum, bismuthum metallicum, cadmium metallicum, calc. fluor., carbo veg., chelidonium majus, cinchona, cobaltum met., cuprum met., glycyrrhiza glabra, hydrofluoricum acidum, iris versicolor, manganum metallicum, merc. viv., niccolum metallicum, osmium metallicum, platinum met., plumb. met., stannum met., strontium carb., thallium metallicum, titanium metallicum, carduus mar., taraxacum. This pharmaceutical product is labeled by Newton Laboratories, Inc. and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 55714-4805-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

Formulated for associated symptoms such as fatigue, headaches, oversensitivity and sluggish elimination.

What are Active Ingredients of this product?

An 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.
  • ACTIVATED CHARCOAL 20 [hp_X]/mL
  • ALUMINUM 20 [hp_X]/mL - A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.
  • BARIUM CARBONATE 20 [hp_X]/mL
  • BERYLLIUM 21 [hp_X]/mL - An element with the atomic symbol Be, atomic number 4, and atomic weight 9.01218. Short exposure to this element can lead to a type of poisoning known as BERYLLIOSIS.
  • BISMUTH 20 [hp_X]/mL - A metallic element that has the atomic symbol Bi, and atomic number 83. Its principal isotope is Bismuth 209.
  • CADMIUM 20 [hp_X]/mL - An element with atomic symbol Cd, atomic number 48, and atomic weight 112.41. It is a metal and ingestion will lead to CADMIUM POISONING.
  • CALCIUM FLUORIDE 20 [hp_X]/mL - Calcium fluoride. Occurring in nature as the mineral fluorite or fluorspar. It is the primary source of fluorine and its compounds. Pure calcium fluoride is used as a catalyst in dehydration and dehydrogenation and is used to fluoridate drinking water. (From Merck Index, 11th ed)
  • CHELIDONIUM MAJUS 20 [hp_X]/mL - A plant species of the family PAPAVERACEAE. The common name greater celandine is similar to lesser celandine (Ficaria verna), and celandine poppy (Stylophorum diphyllum). It has been used in folk medicine and its latex contains biologically active compounds including BENZOPHENANTHRIDINES alkaloids (e.g., Chelerythrine).
  • CINCHONA OFFICINALIS BARK 20 [hp_X]/mL
  • COBALT 20 [hp_X]/mL - A trace element that is a component of vitamin B12. It has the atomic symbol Co, atomic number 27, and atomic weight 58.93. It is used in nuclear weapons, alloys, and pigments. Deficiency in animals leads to anemia; its excess in humans can lead to erythrocytosis.
  • COPPER 20 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
  • GARLIC 20 [hp_X]/mL - A species of Allium used as a spice (SPICES) and traditional remedy. It contains alliin lyase and alliin, which is converted by alliin lyase to allicin, the pungent ingredient responsible for the aroma of fresh cut garlic.
  • GLYCYRRHIZA GLABRA 21 [hp_X]/mL - A genus of leguminous herbs or shrubs whose roots yield GLYCYRRHETINIC ACID and its derivative, CARBENOXOLONE.
  • GOLD 20 [hp_X]/mL - A yellow metallic element with the atomic symbol Au, atomic number 79, and atomic weight 197. It is used in jewelry, goldplating of other metals, as currency, and in dental restoration. Many of its clinical applications, such as ANTIRHEUMATIC AGENTS, are in the form of its salts.
  • HYDROFLUORIC ACID 20 [hp_X]/mL - Hydrofluoric acid. A solution of hydrogen fluoride in water. It is a colorless fuming liquid which can cause painful burns.
  • IRIS VERSICOLOR ROOT 20 [hp_X]/mL
  • LEAD 20 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
  • MANGANESE 20 [hp_X]/mL - A trace element with atomic symbol Mn, atomic number 25, and atomic weight 54.94. It is concentrated in cell mitochondria, mostly in the pituitary gland, liver, pancreas, kidney, and bone, influences the synthesis of mucopolysaccharides, stimulates hepatic synthesis of cholesterol and fatty acids, and is a cofactor in many enzymes, including arginase and alkaline phosphatase in the liver. (From AMA Drug Evaluations Annual 1992, p2035)
  • MERCURY 20 [hp_X]/mL - A silver metallic element that exists as a liquid at room temperature. It has the atomic symbol Hg (from hydrargyrum, liquid silver), atomic number 80, and atomic weight 200.59. Mercury is used in many industrial applications and its salts have been employed therapeutically as purgatives, antisyphilitics, disinfectants, and astringents. It can be absorbed through the skin and mucous membranes which leads to MERCURY POISONING. Because of its toxicity, the clinical use of mercury and mercurials is diminishing.
  • MILK THISTLE 20 [hp_X]/mL
  • NICKEL 20 [hp_X]/mL - A trace element with the atomic symbol Ni, atomic number 28, and atomic weight 58.69. It is a cofactor of the enzyme UREASE.
  • OSMIUM 21 [hp_X]/mL - A very hard, gray, toxic, and nearly infusible metal element, atomic number 76, atomic weight 190.2, symbol Os.
  • PLATINUM 20 [hp_X]/mL - A heavy, soft, whitish metal, resembling tin, with atomic number 78, atomic weight 195.084, symbol Pt. It is used in manufacturing equipment for laboratory and industrial use. It occurs as a black powder (platinum black) and as a spongy substance (spongy platinum) and may have been known in Pliny's time as alutiae.
  • SILVER NITRATE 20 [hp_X]/mL - A silver salt with powerful germicidal activity. It has been used topically to prevent OPHTHALMIA NEONATORUM.
  • STRONTIUM CARBONATE 21 [hp_X]/mL
  • TARAXACUM OFFICINALE 11 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
  • THALLIUM 20 [hp_X]/mL - A heavy, bluish white metal, atomic number 81, atomic weight [204.382; 204.385], symbol Tl.
  • TIN 20 [hp_X]/mL - A trace element that is required in bone formation. It has the atomic symbol Sn, atomic number 50, and atomic weight 118.71.
  • TITANIUM 21 [hp_X]/mL - A dark-gray, metallic element of widespread distribution but occurring in small amounts with atomic number, 22, atomic weight, 47.867 and symbol, Ti; specific gravity, 4.5; used for fixation of fractures.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

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. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
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.
What is the Substance Name? An 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.
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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
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, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".