A05 Heavy Antitox

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

Apex Energetics Inc.
Human Otc Drug
NDC 63479-0105

A05 Heavy Antitox also known as 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 is a human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for A05 Heavy Antitox is 63479-0105. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in A05 Heavy Antitox drug includes Allylthiourea - 12 [hp_X]/mL Aluminum - 30 [hp_X]/mL Apis Mellifera - 4 [hp_X]/mL Atropa Belladonna - 4 [hp_X]/mL Berberis Vulgaris Root Bark - 1 [hp_X]/mL Cadmium - 60 [hp_X]/mL Chelidonium Majus - 1 [hp_X]/mL Copper - 60 [hp_X]/mL Fagus Sylvatica Nut - 2 [hp_X]/mL Formaldehyde - 30 [hp_X]/mL and more. The currest status of A05 Heavy Antitox drug is Active.

Drug Information:

Drug NDC:	63479-0105
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	A05 Heavy Antitox
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base:	A05
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix:	HEAVY ANTITOX
A suffix to the proprietary name, a value here should be appended to the ProprietaryName field to obtain the complete name of the product. This suffix is often used to distinguish characteristics of a product such as extended release (“XR”) or sleep aid (“PM”). Although many companies follow certain naming conventions for suffices, there is no recognized standard.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	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
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Apex Energetics Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Solution/ Drops
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	ALLYLTHIOUREA - 12 [hp_X]/mL ALUMINUM - 30 [hp_X]/mL APIS MELLIFERA - 4 [hp_X]/mL ATROPA BELLADONNA - 4 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 1 [hp_X]/mL CADMIUM - 60 [hp_X]/mL CHELIDONIUM MAJUS - 1 [hp_X]/mL COPPER - 60 [hp_X]/mL FAGUS SYLVATICA NUT - 2 [hp_X]/mL FORMALDEHYDE - 30 [hp_X]/mL Load more... FORMIC ACID - 12 [hp_X]/mL GARLIC - 1 [hp_X]/mL GOLD - 30 [hp_X]/mL HYPERICUM PERFORATUM - 3 [hp_X]/mL ICHTHAMMOL - 10 [hp_X]/mL LEAD - 60 [hp_X]/mL MERCURIC CHLORIDE - 200 [hp_X]/mL MERCURIUS SOLUBILIS - 60 [hp_X]/mL NICKEL - 15 [hp_X]/mL ONION - 1 [hp_X]/mL SELENIUM - 15 [hp_X]/mL SILICON DIOXIDE - 30 [hp_X]/mL SILVER - 60 [hp_X]/mL SOLIDAGO VIRGAUREA FLOWERING TOP - 1 [hp_X]/mL TIN - 30 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	SUBLINGUAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	15 Dec, 1994
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	24 Dec, 2025
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.
Listing Expiration Date:	31 Dec, 2023
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Apex Energetics Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
UPC:	0818960011147
UPC stands for Universal Product Code.
NUI:	N0000185021 N0000175629 N0000184306 N0000185001 M0000728 M0002274 M0005152 N0000175831 N0000008595 N0000008924 N0000175830 N0000185508 N0000185371 M0006342 M0016962 M0022575
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	706IDJ14B7 CPD4NFA903 7S82P3R43Z WQZ3G9PF0H 1TH8Q20J0U 00BH33GNGH 7E889U5RNN 789U1901C5 I57ERU2601 1HG84L3525 Load more... 0YIW783RG1 V1V998DC17 79Y1949PYO XK4IUX8MNB NQ14646378 2P299V784P 53GH7MZT1R 324Y4038G2 7OV03QG267 492225Q21H H6241UJ22B ETJ7Z6XBU4 3M4G523W1G 5405K23S50 387GMG9FH5
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Standardized Insect Venom Allergenic Extract [EPC] Copper-containing Intrauterine Device [EPC] Standardized Chemical Allergen [EPC] Non-Standardized Food Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Inhibit Ovum Fertilization [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Bee Venoms [CS] Copper [CS] Dietary Proteins [CS] Plant Proteins [CS] Vegetable Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Allergens [CS] Bee Venoms [CS] Cell-mediated Immunity [PE] Copper [CS] Copper-containing Intrauterine Device [EPC] Decreased Embryonic Implantation [PE] Decreased Sperm Motility [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Inhibit Ovum Fertilization [PE] Non-Standardized Food Allergenic Extract [EPC] Plant Proteins [CS] Standardized Chemical Allergen [EPC] Standardized Insect Venom Allergenic Extract [EPC] Vegetable Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
63479-0105-1	30 mL in 1 BOTTLE, GLASS (63479-0105-1)	15 Dec, 1994	N/A	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

A05 Heavy Antitox

Allium Cepa & more..

Solution/ Drops
Apex Energetics Inc.
NDC: 63479-0105

Purpose:

Uses: for temporary relief of minor: spasms* fatigue* headache* congestion* dry skin* nervous irritability* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

A05 heavy antitox 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 apis mellifera apis mellifera gold gold hypericum perforatum hypericum perforatum ichthammol ichthammol mercurius solubilis mercurius solubilis lead lead garlic garlic aluminum aluminum atropa belladonna atropa belladonna formaldehyde formaldehyde formic acid formic acid silver silver chelidonium majus chelidonium majus copper copper silicon dioxide silicon dioxide water cadmium cadmium fagus sylvatica nut fagus sylvatica nut berberis vulgaris root bark berberis vulgaris root bark mercuric chloride mercuric cation solidago virgaurea flowering top solidago virgaurea flowering top tin tin allylthiourea allylthiourea onion onion nickel nickel selenium selenium alcohol

Indications and Usage:

Warnings:

Warnings: if pregnant or breastfeeding , ask a health professional before use. do not use if clear seal over the cap is broken or missing. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. stop use and ask a doctor if spasms, fatigue, headache, congestion, dry skin, nervous irritability, or other symptoms do not improve within 7 days or are accompanied by fever.

Dosage and Administration:

Directions: 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.

Stop Use:

Stop use and ask a doctor if spasms, fatigue, headache, congestion, dry skin, nervous irritability, or other symptoms do not improve within 7 days or are accompanied by fever.

Package Label Principal Display Panel:

FutureplexÂ® a05 antitoxÂ® heavy antitoxâ¢ homeopathic formula spasms* fatigue* headache* congestion* 1 fl oz (30 ml) alcohol 20% by volume a0521-0205

Further Questions:

Distributed by apex energetics. questions? 16592 hale ave., irvine, ca 92606, usa

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.