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  4. NDC Product Code: 63479-0105 A05 Heavy Antitox

NDC 63479-0105 A05 Heavy Antitox

Allium Cepa,Allium Sativum,Aluminium Metallicum,Apis Mellifica,Argentum Metallicum,Aurum - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 63479-0105?
  4. A05 Heavy Antitox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

NDC Product Code:
63479-0105
Proprietary Name:
A05 Heavy Antitox
Non-Proprietary Name: [1]
Allium Cepa, Allium Sativum, Aluminium Metallicum, Apis Mellifica, Argentum Metallicum, Aurum Metallicum, Belladonna, Berberis Vulgaris, Cadmium Metallicum, Chelidonium Majus, Cuprum Metallicum, Fagus Sylvatica, Formalinum, Formicum Acidum, Hypericum Perforatum, Ichthyolum, Mercurius Corrosivus, Mercurius Solubilis, Niccolum Metallicum, Plumbum Metallicum, Selenium Metallicum, Silicea, Solidago Virgaurea, Stannum Metallicum, Thiosinaminum
Substance Name: [2]
Allylthiourea; Aluminum; Apis Mellifera; Atropa Belladonna; Berberis Vulgaris Root Bark; Cadmium; Chelidonium Majus; Copper; Fagus Sylvatica Nut; Formaldehyde; Formic Acid; Garlic; Gold; Hypericum Perforatum; Ichthammol; Lead; Mercuric Chloride; Mercurius Solubilis; Nickel; Onion; Selenium; Silicon Dioxide; Silver; Solidago Virgaurea Flowering Top; Tin
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Dosage Form:
Solution/ Drops - A solution which is usually administered in a drop-wise fashion.
Administration Route(s): [4]
  • Sublingual - Administration beneath the tongue.
    • Labeler Name: [5]
    Apex Energetics Inc.
    Labeler Code:
    63479
    Product Label ID:
    b9bdc39e-8ebf-615c-e053-2a95a90afe1b
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    12-15-1994
    Listing Expiration Date: [11]
    12-31-2025
    Exclude Flag: [12]
    N
    Code Navigator:

    Code Structure Chart

    Product Details

    What is NDC 63479-0105?

    The NDC code 63479-0105 is assigned by the FDA to the product A05 Heavy Antitox which is a human over the counter drug product labeled by Apex Energetics Inc.. The generic name of A05 Heavy Antitox is allium cepa, allium sativum, aluminium metallicum, apis mellifica, argentum metallicum, aurum metallicum, belladonna, berberis vulgaris, cadmium metallicum, chelidonium majus, cuprum metallicum, fagus sylvatica, formalinum, formicum acidum, hypericum perforatum, ichthyolum, mercurius corrosivus, mercurius solubilis, niccolum metallicum, plumbum metallicum, selenium metallicum, silicea, solidago virgaurea, stannum metallicum, thiosinaminum. The product's dosage form is solution/ drops and is administered via sublingual form. The product is distributed in a single package with assigned NDC code 63479-0105-1 30 ml in 1 bottle, glass . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

    What are the uses for A05 Heavy Antitox?

    Adults & children ages 12 years and over: Take 10 drops under the tongue 3 times a day, or as directed by your healthcare professional. Consult a physician for use in children under 12 years of age.

    What are A05 Heavy Antitox Active Ingredients?

    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.
    • ALLYLTHIOUREA 12 [hp_X]/mL
    • ALUMINUM 30 [hp_X]/mL - A metallic element that has the atomic number 13, atomic symbol Al, and atomic weight 26.98.
    • APIS MELLIFERA 4 [hp_X]/mL
    • ATROPA BELLADONNA 4 [hp_X]/mL - A plant species of the genus ATROPA, family SOLANACEAE that contains ATROPINE; SCOPOLAMINE; BELLADONNA ALKALOIDS and other SOLANACEOUS ALKALOIDS. Some species in this genus are called deadly nightshade which is also a common name for SOLANUM.
    • BERBERIS VULGARIS ROOT BARK 1 [hp_X]/mL
    • CADMIUM 60 [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.
    • CHELIDONIUM MAJUS 1 [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).
    • COPPER 60 [hp_X]/mL - A heavy metal trace element with the atomic symbol Cu, atomic number 29, and atomic weight 63.55.
    • FAGUS SYLVATICA NUT 2 [hp_X]/mL
    • FORMALDEHYDE 30 [hp_X]/mL - A highly reactive aldehyde gas formed by oxidation or incomplete combustion of hydrocarbons. In solution, it has a wide range of uses: in the manufacture of resins and textiles, as a disinfectant, and as a laboratory fixative or preservative. Formaldehyde solution (formalin) is considered a hazardous compound, and its vapor toxic. (From Reynolds, Martindale The Extra Pharmacopoeia, 30th ed, p717)
    • FORMIC ACID 12 [hp_X]/mL
    • GARLIC 1 [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.
    • GOLD 30 [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.
    • HYPERICUM PERFORATUM 3 [hp_X]/mL
    • ICHTHAMMOL 10 [hp_X]/mL
    • LEAD 60 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.
    • MERCURIC CHLORIDE 200 [hp_X]/mL - Mercury chloride (HgCl2). A highly toxic compound that volatizes slightly at ordinary temperature and appreciably at 100 degrees C. It is corrosive to mucous membranes and used as a topical antiseptic and disinfectant.
    • MERCURIUS SOLUBILIS 60 [hp_X]/mL
    • NICKEL 15 [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.
    • ONION 1 [hp_X]/mL - Herbaceous biennial plants and their edible bulbs, belonging to the Allium genus.
    • SELENIUM 15 [hp_X]/mL - An element with the atomic symbol Se, atomic number 34, and atomic weight 78.97. It is an essential micronutrient for mammals and other animals but is toxic in large amounts. Selenium protects intracellular structures against oxidative damage. It is an essential component of GLUTATHIONE PEROXIDASE.
    • SILICON DIOXIDE 30 [hp_X]/mL - Transparent, tasteless crystals found in nature as agate, amethyst, chalcedony, cristobalite, flint, sand, QUARTZ, and tridymite. The compound is insoluble in water or acids except hydrofluoric acid.
    • SILVER 60 [hp_X]/mL - An element with the atomic symbol Ag, atomic number 47, and atomic weight 107.87. It is a soft metal that is used medically in surgical instruments, dental prostheses, and alloys. Long-continued use of silver salts can lead to a form of poisoning known as ARGYRIA.
    • SOLIDAGO VIRGAUREA FLOWERING TOP 1 [hp_X]/mL
    • TIN 30 [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.

    Which are A05 Heavy Antitox UNII Codes?

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

    Which are A05 Heavy Antitox Inactive Ingredients 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 for A05 Heavy Antitox?

    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.

    * Please review the disclaimer below.

    Product Footnotes

    [1] 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.

    [2] 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.

    [3] 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.

    [4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.

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

    [8] 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.

    [9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

    [11] 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.

    [12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".