NDC 57955-0281 Heavy Metal Detox

Alumina, Arsenicum Album, Arsenicum Lodatum, Berberis Vulgaris, Cadmium Sulphuratum, Chelidonium Majus, Chromium Oxydatum, Cuprum Metallicum, Cysteinum, Glycerinum, Glycyrrhiza Glabra, Kali Muriaticum, Magnesia Sulphurica, Mercurius Corrosivus, Mercurius Cyanatus, Mercurius Dulcis, Mezereum, Natrum Muriaticum, Niccolum Metallicum, Oleum Morrhuae, Phytolacca Decandra, Plumbum Iodatum, Plumbum Metallicum, Selenium Metallicum, Solidago Virgaurea, Stannum Metallicum

NDC Product Code 57955-0281

NDC Code: 57955-0281

Proprietary Name: Heavy Metal 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: Alumina, Arsenicum Album, Arsenicum Lodatum, Berberis Vulgaris, Cadmium Sulphuratum, Chelidonium Majus, Chromium Oxydatum, Cuprum Metallicum, Cysteinum, Glycerinum, Glycyrrhiza Glabra, Kali Muriaticum, Magnesia Sulphurica, Mercurius Corrosivus, Mercurius Cyanatus, Mercurius Dulcis, Mezereum, Natrum Muriaticum, Niccolum Metallicum, Oleum Morrhuae, Phytolacca Decandra, Plumbum Iodatum, Plumbum Metallicum, Selenium Metallicum, Solidago Virgaurea, Stannum Metallicum 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

  • 57955 - King Bio Inc.
    • 57955-0281 - Heavy Metal Detox

NDC 57955-0281-2

Package Description: 59 mL in 1 BOTTLE, SPRAY

NDC Product Information

Heavy Metal Detox with NDC 57955-0281 is a a human over the counter drug product labeled by King Bio Inc.. The generic name of Heavy Metal Detox is alumina, arsenicum album, arsenicum lodatum, berberis vulgaris, cadmium sulphuratum, chelidonium majus, chromium oxydatum, cuprum metallicum, cysteinum, glycerinum, glycyrrhiza glabra, kali muriaticum, magnesia sulphurica, mercurius corrosivus, mercurius cyanatus, mercurius dulcis, mezereum, natrum muriaticum, niccolum metallicum, oleum morrhuae, phytolacca decandra, plumbum iodatum, plumbum metallicum, selenium metallicum, solidago virgaurea, stannum metallicum. The product's dosage form is liquid and is administered via oral form.

Labeler Name: King Bio Inc.

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.

Heavy Metal 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.

  • ALUMINUM OXIDE 10 [hp_X]/59mL
  • ARSENIC TRIOXIDE 10 [hp_X]/59mL
  • ARSENIC TRIIODIDE 10 [hp_X]/59mL
  • BERBERIS VULGARIS ROOT BARK 10 [hp_X]/59mL
  • CADMIUM SULFIDE 10 [hp_X]/59mL
  • CHELIDONIUM MAJUS 10 [hp_X]/59mL
  • CHROMIC OXIDE 10 [hp_X]/59mL
  • COPPER 10 [hp_X]/59mL
  • CYSTEINE 10 [hp_X]/59mL
  • GLYCERIN 10 [hp_X]/59mL
  • GLYCYRRHIZA GLABRA 10 [hp_X]/59mL
  • POTASSIUM CHLORIDE 10 [hp_X]/59mL
  • MAGNESIUM SULFATE HEPTAHYDRATE 10 [hp_X]/59mL
  • MERCURIC CHLORIDE 10 [hp_X]/59mL
  • MERCURIC CYANIDE 10 [hp_X]/59mL
  • CALOMEL 10 [hp_X]/59mL
  • DAPHNE MEZEREUM BARK 10 [hp_X]/59mL
  • SODIUM CHLORIDE 10 [hp_X]/59mL
  • NICKEL 10 [hp_X]/59mL
  • COD LIVER OIL 10 [hp_X]/59mL
  • PHYTOLACCA AMERICANA ROOT 10 [hp_X]/59mL
  • LEAD IODIDE 10 [hp_X]/59mL
  • LEAD 10 [hp_X]/59mL
  • SELENIUM 10 [hp_X]/59mL
  • SOLIDAGO VIRGAUREA FLOWERING TOP 10 [hp_X]/59mL
  • TIN 10 [hp_X]/59mL

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)
  • POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
  • ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)

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: King Bio Inc.
Labeler Code: 57955
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: 08-21-2015 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: 12-31-2018 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: E 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 Detox Product Label Images

Heavy Metal 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

Otc - Active Ingredient

Drug Facts​__________________________________________________________________________________________________________HPUS active ingredients: ​Alumina, Arsenicum album, Arsenicum iodatum, Berberis vulgaris, Cadmium sulphuratum, Chelidonium majus, Chromium oxydatum, Cuprum metallicum, Cysteinum, Glycerinum, Glycyrrhiza glabra, Kali muriaticum, Magnesia sulphurica, Mercurius corrosivus, Mercurius cyanatus, Mercurius dulcis, Mezereum, Natrum muriaticum, Niccolum metallicum, Oleum morrhuae, Phytolacca decandra, Plumbum iodatum, Plumbum metallicum, Selenium metallicum, Solidago virgaurea, Stannum metallicum. Equal volumes of each ingredient in 10X, 30X, 100X, LM1, LM2, LM3, LM5 potencies.

Indications & Usage

Uses for symptomatic relief of heavy metal toxicity, such as: fatigue, metallic taste in mouth, poor digestion.

Inactive Ingredient

Inactive Ingredients: Bio-Energetically Enhanced™ pure water, citric acid and potassium sorbate.

Warnings

  • WarningsStop use and ask your doctor if symptoms persist or worsen.If pregnant or breast-feeding, take only on advice of a healthcare professional.

Otc - Keep Out Of Reach Of Children

  • Keep out of reach of children.

Dosage & Administration

  • DirectionsInitially, depress pump until primed.Spray one dose directly into mouth.Adults 12 and up: 3 sprays 3 times per day.​Children 2-12: 2 sprays 3 times per day.Children 2 mo-2yr: 1 spray 3 times per day.

Other Safety Information

Tamper resistant for your protection. Use only if safety seal is intact. This product has not been clinically tested.

Otc - Purpose

  • Uses ​for symptomatic relief of heavy metal toxicity, such as: fatiguemetallic taste in mouthpoor digestion

* Please review the disclaimer below.

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