B09 Acute Virotox

Aconitum Napellus, Arsenicum Album, Baptisia Tinctoria, Belladonna, Bryonia, Cherry Plum, Clematis Vitalba, Echinacea Angustifolia, Echinacea Purpurea, Eucalyptus Globulus, Eupatorium Perfoliatum, European Olive, Ferrum Phosphoricum, Gentiana Lutea, Impatiens Glandulifera, Influenza A Virus, Lachesis Mutus, Luffa Operculata, Ornithogalum Umbellatum, Phosphorus, Rockrose, Sarcolacticum Acidum, Veratrum Album, Yellow Jasmine


Apex Energetics Inc.
Human Otc Drug
NDC 63479-0209
B09 Acute Virotox also known as Aconitum Napellus, Arsenicum Album, Baptisia Tinctoria, Belladonna, Bryonia, Cherry Plum, Clematis Vitalba, Echinacea Angustifolia, Echinacea Purpurea, Eucalyptus Globulus, Eupatorium Perfoliatum, European Olive, Ferrum Phosphoricum, Gentiana Lutea, Impatiens Glandulifera, Influenza A Virus, Lachesis Mutus, Luffa Operculata, Ornithogalum Umbellatum, Phosphorus, Rockrose, Sarcolacticum Acidum, Veratrum Album, Yellow Jasmine is a human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for B09 Acute Virotox is 63479-0209. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in B09 Acute Virotox drug includes Aconitum Napellus - 200 [hp_X]/mL Arsenic Trioxide - 200 [hp_X]/mL Atropa Belladonna - 200 [hp_X]/mL Baptisia Tinctoria Root - 9 [hp_X]/mL Bryonia Alba Root - 200 [hp_X]/mL Clematis Vitalba Flower - 9 [hp_X]/mL Echinacea Angustifolia - 1 [hp_X]/mL Echinacea Purpurea - 1 [hp_X]/mL Eucalyptus Globulus Leaf - 12 [hp_X]/mL Eupatorium Perfoliatum Flowering Top - 3 [hp_X]/mL and more. The currest status of B09 Acute Virotox drug is Active.

Drug Information:

Drug NDC: 63479-0209
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: B09 Acute Virotox
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: B09
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: ACUTE VIROTOX
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: Aconitum Napellus, Arsenicum Album, Baptisia Tinctoria, Belladonna, Bryonia, Cherry Plum, Clematis Vitalba, Echinacea Angustifolia, Echinacea Purpurea, Eucalyptus Globulus, Eupatorium Perfoliatum, European Olive, Ferrum Phosphoricum, Gentiana Lutea, Impatiens Glandulifera, Influenza A Virus, Lachesis Mutus, Luffa Operculata, Ornithogalum Umbellatum, Phosphorus, Rockrose, Sarcolacticum Acidum, Veratrum Album, Yellow Jasmine
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:ACONITUM NAPELLUS - 200 [hp_X]/mL
ARSENIC TRIOXIDE - 200 [hp_X]/mL
ATROPA BELLADONNA - 200 [hp_X]/mL
BAPTISIA TINCTORIA ROOT - 9 [hp_X]/mL
BRYONIA ALBA ROOT - 200 [hp_X]/mL
CLEMATIS VITALBA FLOWER - 9 [hp_X]/mL
ECHINACEA ANGUSTIFOLIA - 1 [hp_X]/mL
ECHINACEA PURPUREA - 1 [hp_X]/mL
EUCALYPTUS GLOBULUS LEAF - 12 [hp_X]/mL
EUPATORIUM PERFOLIATUM FLOWERING TOP - 3 [hp_X]/mL
FERROSOFERRIC PHOSPHATE - 200 [hp_X]/mL
GELSEMIUM SEMPERVIRENS ROOT - 30 [hp_X]/mL
GENTIANA LUTEA ROOT - 6 [hp_X]/mL
HELIANTHEMUM NUMMULARIUM FLOWER - 9 [hp_X]/mL
IMPATIENS GLANDULIFERA FLOWER - 9 [hp_X]/mL
INFLUENZA A VIRUS WHOLE - 30 [hp_X]/mL
LACHESIS MUTA VENOM - 30 [hp_X]/mL
LACTIC ACID, L- - 12 [hp_X]/mL
LUFFA OPERCULATA FRUIT - 12 [hp_X]/mL
OLEA EUROPAEA FLOWER - 9 [hp_X]/mL
ORNITHOGALUM UMBELLATUM FLOWERING TOP - 9 [hp_X]/mL
PHOSPHORUS - 30 [hp_X]/mL
PRUNUS CERASIFERA FLOWER - 9 [hp_X]/mL
VERATRUM ALBUM ROOT - 12 [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: 20 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.
UNII:U0NQ8555JD
S7V92P67HO
WQZ3G9PF0H
5EF0HWI5WU
T7J046YI2B
7SCP4N87CI
VB06AV5US8
QI7G114Y98
S546YLW6E6
1W0775VX6E
91GQH8I5F7
639KR60Q1Q
S72O3284MS
51BRR32WPP
AJU5O1A5ZV
R9HH0NDE2E
VSW71SS07I
F9S9FFU82N
C4MO6809HU
498M34P1VZ
CZD6M4PY4B
27YLU75U4W
0KD7R09EAS
QNS6W5US1Z
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.

Packaging Information:

Package NDCDescriptionMarketing Start DateMarketing End DateSample Available
63479-0209-130 mL in 1 BOTTLE, GLASS (63479-0209-1)15 Dec, 1994N/ANo
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.

Purpose:

Uses: for temporary relief of minor: chills* muscle aches* fatigue* upset stomach* nausea* nervous irritability* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

B09 acute virotox aconitum napellus, arsenicum album, baptisia tinctoria, belladonna, bryonia, cherry plum, clematis vitalba, echinacea angustifolia, echinacea purpurea, eucalyptus globulus, eupatorium perfoliatum, european olive, ferrum phosphoricum, gentiana lutea, impatiens glandulifera, influenza a virus, lachesis mutus, luffa operculata, ornithogalum umbellatum, phosphorus, rockrose, sarcolacticum acidum, veratrum album, yellow jasmine echinacea angustifolia echinacea angustifolia aconitum napellus aconitum napellus prunus cerasifera flower prunus cerasifera flower phosphorus phosphorus helianthemum nummularium flower helianthemum nummularium flower baptisia tinctoria root baptisia tinctoria root clematis vitalba flower clematis vitalba flower eucalyptus globulus leaf eucalyptus globulus leaf bryonia alba root bryonia alba root ferrosoferric phosphate ferrosoferric phosphate water atropa belladonna atropa belladonna arsenic trioxide arsenic cation (3+) gelsemium sempervirens root gelsemium sempervirens root gentiana lutea root gentiana lutea root impatiens glandulifera flower impatiens glandulifera flower lachesis muta venom lachesis muta venom lactic acid, l- lactic acid, l- veratrum album root veratrum album root alcohol eupatorium perfoliatum flowering top eupatorium perfoliatum flowering top olea europaea flower olea europaea flower influenza a virus whole influenza a virus whole luffa operculata fruit luffa operculata fruit echinacea purpurea echinacea purpurea ornithogalum umbellatum flowering top ornithogalum umbellatum flowering top

Indications and Usage:

Uses: for temporary relief of minor: chills* muscle aches* fatigue* upset stomach* nausea* nervous irritability* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

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 chills, muscle aches, fatigue, upset stomach, nausea, 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 5-8 drops under the tongue 3-4 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 chills, muscle aches, fatigue, upset stomach, nausea, nervous irritability, or other symptoms do not improve within 7 days or are accompanied by fever.

Package Label Principal Display Panel:

Futureplex® b09 antitox® acute virotox™ homeopathic formula chills* muscle aches* fatigue* 1 fl oz (30 ml) alcohol 20% by volume b09 acute virotox 20210302 lable.jpg

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.