B11 Injurotox

Aristolochia Milhomens, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia, Calendula Officinalis, Carbo Vegetabilis, Chamomilla, Cherry Plum Flower, Clematis Vitalba Flower, Echinacea Angustifolia, Hamamelis Virginiana, Hepar Sulphuris Calcareum, Hypericum Perforatum, Impatiens Glandulifera Flower, Lachesis Mutus, Millefolium, Pyrenees Star Of Bethlehem, Rhus Toxicodendron, Rockrose Flower, Ruta Graveolens, Sarcolacticum Acidum, Sulphur Iodatum, Symphytum Officinale, Veratrum Album


Apex Energetics Inc.
Human Otc Drug
NDC 63479-0211
B11 Injurotox also known as Aristolochia Milhomens, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia, Calendula Officinalis, Carbo Vegetabilis, Chamomilla, Cherry Plum Flower, Clematis Vitalba Flower, Echinacea Angustifolia, Hamamelis Virginiana, Hepar Sulphuris Calcareum, Hypericum Perforatum, Impatiens Glandulifera Flower, Lachesis Mutus, Millefolium, Pyrenees Star Of Bethlehem, Rhus Toxicodendron, Rockrose Flower, Ruta Graveolens, Sarcolacticum Acidum, Sulphur Iodatum, Symphytum Officinale, Veratrum Album is a human otc drug labeled by 'Apex Energetics Inc.'. National Drug Code (NDC) number for B11 Injurotox is 63479-0211. This drug is available in dosage form of Solution/ Drops. The names of the active, medicinal ingredients in B11 Injurotox drug includes Achillea Millefolium - 1 [hp_X]/mL Activated Charcoal - 12 [hp_X]/mL Aristolochia Cymbifera Flower - 9 [hp_X]/mL Arnica Montana - 100 [hp_X]/mL Arsenic Trioxide - 30 [hp_X]/mL Atropa Belladonna - 8 [hp_X]/mL Bellis Perennis - 1 [hp_X]/mL Bryonia Alba Root - 30 [hp_X]/mL Calcium Sulfide - 30 [hp_X]/mL Calendula Officinalis Flowering Top - 1 [hp_X]/mL and more. The currest status of B11 Injurotox drug is Active.

Drug Information:

Drug NDC: 63479-0211
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: B11 Injurotox
Also known as the trade name. It is the name of the product chosen by the labeler.
Proprietary Name Base: B11
The base of the Brand/Proprietary name excluding its suffix.
Proprietary Name Suffix: INJUROTOX
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: Aristolochia Milhomens, Arnica Montana, Arsenicum Album, Belladonna, Bellis Perennis, Bryonia, Calendula Officinalis, Carbo Vegetabilis, Chamomilla, Cherry Plum Flower, Clematis Vitalba Flower, Echinacea Angustifolia, Hamamelis Virginiana, Hepar Sulphuris Calcareum, Hypericum Perforatum, Impatiens Glandulifera Flower, Lachesis Mutus, Millefolium, Pyrenees Star Of Bethlehem, Rhus Toxicodendron, Rockrose Flower, Ruta Graveolens, Sarcolacticum Acidum, Sulphur Iodatum, Symphytum Officinale, Veratrum Album
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:ACHILLEA MILLEFOLIUM - 1 [hp_X]/mL
ACTIVATED CHARCOAL - 12 [hp_X]/mL
ARISTOLOCHIA CYMBIFERA FLOWER - 9 [hp_X]/mL
ARNICA MONTANA - 100 [hp_X]/mL
ARSENIC TRIOXIDE - 30 [hp_X]/mL
ATROPA BELLADONNA - 8 [hp_X]/mL
BELLIS PERENNIS - 1 [hp_X]/mL
BRYONIA ALBA ROOT - 30 [hp_X]/mL
CALCIUM SULFIDE - 30 [hp_X]/mL
CALENDULA OFFICINALIS FLOWERING TOP - 1 [hp_X]/mL
CLEMATIS VITALBA FLOWER - 9 [hp_X]/mL
COMFREY ROOT - 2 [hp_X]/mL
ECHINACEA ANGUSTIFOLIA - 1 [hp_X]/mL
HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK - 1 [hp_X]/mL
HELIANTHEMUM NUMMULARIUM FLOWER - 9 [hp_X]/mL
HYPERICUM PERFORATUM - 3 [hp_X]/mL
IMPATIENS GLANDULIFERA FLOWER - 9 [hp_X]/mL
LACHESIS MUTA VENOM - 30 [hp_X]/mL
LACTIC ACID, L- - 30 [hp_X]/mL
MATRICARIA CHAMOMILLA - 30 [hp_X]/mL
ORNITHOGALUM UMBELLATUM FLOWERING TOP - 9 [hp_X]/mL
PRUNUS CERASIFERA FLOWER - 9 [hp_X]/mL
RUTA GRAVEOLENS FLOWERING TOP - 3 [hp_X]/mL
SULFUR IODIDE - 12 [hp_X]/mL
TOXICODENDRON PUBESCENS LEAF - 30 [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: 13 Jun, 2026
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:2FXJ6SW4PK
2P3VWU3H10
R06VWT372T
O80TY208ZW
S7V92P67HO
WQZ3G9PF0H
2HU33I03UY
T7J046YI2B
1MBW07J51Q
18E7415PXQ
7SCP4N87CI
M9VVZ08EKQ
VB06AV5US8
T7S323PKJS
51BRR32WPP
XK4IUX8MNB
AJU5O1A5ZV
VSW71SS07I
F9S9FFU82N
G0R4UBI2ZZ
CZD6M4PY4B
0KD7R09EAS
N94C2U587S
L6L8KA2AA0
6IO182RP7A
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
63479-0211-130 mL in 1 BOTTLE, GLASS (63479-0211-1)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: joint pain* bruises* swelling* headache* muscle pain* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

Product Elements:

B11 injurotox aristolochia milhomens, arnica montana, arsenicum album, belladonna, bellis perennis, bryonia, calendula officinalis, carbo vegetabilis, chamomilla, cherry plum flower, clematis vitalba flower, echinacea angustifolia, hamamelis virginiana, hepar sulphuris calcareum, hypericum perforatum, impatiens glandulifera flower, lachesis mutus, millefolium, pyrenees star of bethlehem, rhus toxicodendron, rockrose flower, ruta graveolens, sarcolacticum acidum, sulphur iodatum, symphytum officinale, veratrum album aristolochia cymbifera flower aristolochia cymbifera flower arnica montana arnica montana arsenic trioxide arsenic cation (3+) bellis perennis bellis perennis achillea millefolium achillea millefolium whole ruta graveolens flowering top ruta graveolens flowering top lactic acid, l- lactic acid, l- comfrey root comfrey root impatiens glandulifera flower impatiens glandulifera flower activated charcoal activated charcoal matricaria chamomilla matricaria chamomilla whole prunus cerasifera flower prunus cerasifera flower clematis vitalba flower clematis vitalba flower echinacea angustifolia echinacea angustifolia whole helianthemum nummularium flower helianthemum nummularium flower veratrum album root veratrum album root ornithogalum umbellatum flowering top ornithogalum umbellatum flowering top toxicodendron pubescens leaf toxicodendron pubescens leaf atropa belladonna atropa belladonna calendula officinalis flowering top calendula officinalis flowering top hamamelis virginiana root bark/stem bark hamamelis virginiana root bark/stem bark calcium sulfide calcium sulfide lachesis muta venom lachesis muta venom sulfur iodide sulfur iodide alcohol water bryonia alba root bryonia alba root hypericum perforatum hypericum perforatum whole

Indications and Usage:

Uses: for temporary relief of minor: joint pain* bruises* swelling* headache* muscle pain* *claims based on traditional homeopathic practice, not accepted medical evidence. not fda evaluated.

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 joint pain, bruises, swelling, headache, muscle pain, 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: take10 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 joint pain, bruises, swelling, headache, muscle pain, or other symptoms do not improve within 7 days or are accompanied by fever.

Package Label Principal Display Panel:

Futureplex® b11 antitox® injurotox™ homeopathic formula joint pain* bruises* swelling* 1 fl oz (30 ml) alcohol 20% by volume b11 injurotox label.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.