NDC 55714-4561 Heavy Metal - Amalga Detox

Allium Sat., Alumin Met., Arg. Met., Aur. Met., Baryta Carb., Beryllium, Bismuthum Met., Cadmium Met., Calc. Fluor., Carbo Veg., Chelidonium Maj., Cinchona, Cobaltum Met., Cuprum Met., Glycyrrhiza, Hydrofluoricum Ac., Iris Versicolor, Mang Met., Merc. Viv., Niccolum Met., Osmium Met., Platinum Met., Plumb. Met., Stannum Met., Strontium Carb., Thallium Met., Titanium Met., Carduus Mar., Taraxacum

NDC Product Code 55714-4561

NDC Code: 55714-4561

Proprietary Name: Heavy Metal - Amalga Detox 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 Sat., Alumin Met., Arg. Met., Aur. Met., Baryta Carb., Beryllium, Bismuthum Met., Cadmium Met., Calc. Fluor., Carbo Veg., Chelidonium Maj., Cinchona, Cobaltum Met., Cuprum Met., Glycyrrhiza, Hydrofluoricum Ac., Iris Versicolor, Mang Met., Merc. Viv., Niccolum Met., Osmium Met., Platinum Met., Plumb. Met., Stannum Met., Strontium Carb., Thallium Met., Titanium Met., Carduus Mar., Taraxacum 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

  • 55714 - Newton Laboratories, Inc.
    • 55714-4561 - Heavy Metal - Amalga Detox

NDC 55714-4561-1

Package Description: 28.35 g in 1 BOTTLE, GLASS

NDC 55714-4561-2

Package Description: 56.7 g in 1 BOTTLE, GLASS

NDC Product Information

Heavy Metal - Amalga Detox with NDC 55714-4561 is a a human prescription drug product labeled by Newton Laboratories, Inc.. The generic name of Heavy Metal - Amalga Detox is allium sat., alumin met., arg. met., aur. met., baryta carb., beryllium, bismuthum met., cadmium met., calc. fluor., carbo veg., chelidonium maj., cinchona, cobaltum met., cuprum met., glycyrrhiza, hydrofluoricum ac., iris versicolor, mang met., merc. viv., niccolum met., osmium met., platinum met., plumb. met., stannum met., strontium carb., thallium met., titanium met., carduus mar., taraxacum. The product's dosage form is pellet and is administered via oral form.

Labeler Name: Newton Laboratories, Inc.

Dosage Form: Pellet - A small sterile solid mass consisting of a highly purified drug (with or without excipients) made by the formation of granules, or by compression and molding.

Product Type: Human Prescription 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.

Heavy Metal - Amalga Detox 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 20 [hp_X]/g
  • ALUMINUM 20 [hp_X]/g
  • SILVER 20 [hp_X]/g
  • GOLD 20 [hp_X]/g
  • BARIUM CARBONATE 20 [hp_X]/g
  • BERYLLIUM 20 [hp_X]/g
  • BISMUTH 20 [hp_X]/g
  • CADMIUM 20 [hp_X]/g
  • CALCIUM FLUORIDE 20 [hp_X]/g
  • ACTIVATED CHARCOAL 20 [hp_X]/g
  • CHELIDONIUM MAJUS 20 [hp_X]/g
  • CINCHONA OFFICINALIS BARK 20 [hp_X]/g
  • COBALT 20 [hp_X]/g
  • COPPER 20 [hp_X]/g
  • GLYCYRRHIZA GLABRA 20 [hp_X]/g
  • HYDROFLUORIC ACID 20 [hp_X]/g
  • IRIS VERSICOLOR ROOT 20 [hp_X]/g
  • MANGANESE 20 [hp_X]/g
  • MERCURY 20 [hp_X]/g
  • NICKEL 20 [hp_X]/g
  • OSMIUM 20 [hp_X]/g
  • PLATINUM 20 [hp_X]/g
  • LEAD 20 [hp_X]/g
  • TIN 20 [hp_X]/g
  • STRONTIUM CARBONATE 20 [hp_X]/g
  • THALLIUM 20 [hp_X]/g
  • TITANIUM 20 [hp_X]/g
  • SILYBUM MARIANUM SEED 8 [hp_X]/g
  • TARAXACUM OFFICINALE 8 [hp_X]/g

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.

  • SUCROSE (UNII: C151H8M554)

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.

Pharmacological Class(es)

What is a Pharmacological Class?
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Dietary Proteins - [CS]
  • Plant Proteins - [CS]
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Copper - [CS]
  • Copper-containing Intrauterine Device - [EPC] (Established Pharmacologic Class)
  • Decreased Embryonic Implantation - [PE] (Physiologic Effect)
  • Decreased Sperm Motility - [PE] (Physiologic Effect)
  • Inhibit Ovum Fertilization - [PE] (Physiologic Effect)
  • Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Allergens - [CS]
  • Dietary Proteins - [CS]
  • Plant Proteins - [CS]
  • Standardized Chemical Allergen - [EPC] (Established Pharmacologic Class)
  • Increased Histamine Release - [PE] (Physiologic Effect)
  • Cell-mediated Immunity - [PE] (Physiologic Effect)
  • Allergens - [CS]

Product Labeler Information

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

Labeler Name: Newton Laboratories, Inc.
Labeler Code: 55714
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: 06-01-2011 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

Listing Expiration Date: 12-31-2019 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.

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.

Heavy Metal - Amalga Detox Product Label Images

Heavy Metal - Amalga Detox 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

Indications & Usage Section

Heavy Metal - Amalga Detox  Formulated for symptoms of heavy metal and amalgam exposure such as fatigue, headaches, compromised immunity and sluggish elimination.

Dosage & Administration Section

Directions:   Ages 12 and up, take 6 pellets orally (ages 0 to 11, give 3 pellets) one to four times daily or as directed by a healthcare professional.  Under age 2, crush or dissolve pellets in purified water.

Active Ingredient Section

Allium sativum 20x, Aluminium metallicum 20x, Arg. met. 20x, Aur. met. 20x, Baryta carb. 20x, Beryllium metallicum 20x, Bismuthum metallicum 20x, Cadmium metallicum 20x, Calc. fluor. 20x, Carbo veg. 20x, Chelidonium majus 20x, Cinchona 20x, Cobaltum met. 20x, Cuprum met. 20x, Glycyrrhiza glabra 20x, Hydrofluoricum acidum 20x, Iris versicolor 20x, Manganum metallicum 20x, Merc. viv. 20x, Niccolum metallicum 20x, Osmium metallicum 20x, Platinum met. 20x, Plumb. met. 20x, Stannum met. 20x, Strontium carb. 20x, Thallium metallicum 20x, Titanium metallicum 20x, Carduus mar. 8x, Iris versicolor 8x, Taraxacum 8x, Carduus mar. 3x, Iris versicolor 3x, Taraxacum 3x.

Purpose Section

Formulated for symptoms of heavy metal and amalgam exposure such as fatigue, headaches, compromised immunity and sluggish elimination.

Inactive Ingredient Section

Inactive Ingredients:  Gluten-free, non-GMO, beet-derived sucrose pellets.

Questions? Section

Www.newtonlabs.net  Newton Laboratories, Inc. FDA Est # 1051203 - Conyers, GA 30012Questions?  1.800.448.7256

Warnings Section

Warning:  Do not use if tamper - evident seal is broken or missing.  Consult a licensed healthcare professional if pregnant, nursing or if symptoms worsen or persist for more than a few days.  Keep out of reach of children.

Pregnancy Or Breast Feeding Section

Consult a licensed healthcare professional if pregnant or nursing or if symptoms worsen or persist for more than a few days.

Keep Out Of Reach Of Children Section

Keep out of reach of children.

* Please review the disclaimer below.

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