Industrotox

Glycyrrhiza Glabra, Plantago Major, Stillingia Sylvatica, Trifolium Pratense, Arnica Montana, Asclepias Tuberosa, Berberis Vulgaris, Calendula Officinalis, Chamomilla, Chelidonium Majus, Echinacea (angustifolia), Eucalyptus Globulus, Lappa Major, Nasturtium Aquaticum, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Taraxacum Officinale, Trigonella Foenum-graecum, Urtica Dioica, Xanthoxylum Fraxineum, Symphytum Officinale, Hepar Suis, Lung (suis), Lymph Node (suis)

Bioactive Nutritional, Inc.
Human Otc Drug
NDC 43857-0451

Industrotox also known as Glycyrrhiza Glabra, Plantago Major, Stillingia Sylvatica, Trifolium Pratense, Arnica Montana, Asclepias Tuberosa, Berberis Vulgaris, Calendula Officinalis, Chamomilla, Chelidonium Majus, Echinacea (angustifolia), Eucalyptus Globulus, Lappa Major, Nasturtium Aquaticum, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Taraxacum Officinale, Trigonella Foenum-graecum, Urtica Dioica, Xanthoxylum Fraxineum, Symphytum Officinale, Hepar Suis, Lung (suis), Lymph Node (suis) is a human otc drug labeled by 'Bioactive Nutritional, Inc.'. National Drug Code (NDC) number for Industrotox is 43857-0451. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Industrotox drug includes Arctium Lappa Root - 4 [hp_X]/mL Arnica Montana - 3 [hp_X]/mL Asclepias Tuberosa Root - 4 [hp_X]/mL Atropa Belladonna - 12 [hp_X]/mL Berberis Vulgaris Root Bark - 4 [hp_X]/mL Calendula Officinalis Flowering Top - 4 [hp_X]/mL Chelidonium Majus - 4 [hp_X]/mL Comfrey Root - 6 [hp_X]/mL Echinacea Angustifolia - 4 [hp_X]/mL Eucalyptus Globulus Leaf - 4 [hp_X]/mL and more. The currest status of Industrotox drug is Active.

Drug Information:

Drug NDC:	43857-0451
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:	Industrotox
Also known as the trade name. It is the name of the product chosen by the labeler.
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:	Glycyrrhiza Glabra, Plantago Major, Stillingia Sylvatica, Trifolium Pratense, Arnica Montana, Asclepias Tuberosa, Berberis Vulgaris, Calendula Officinalis, Chamomilla, Chelidonium Majus, Echinacea (angustifolia), Eucalyptus Globulus, Lappa Major, Nasturtium Aquaticum, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Taraxacum Officinale, Trigonella Foenum-graecum, Urtica Dioica, Xanthoxylum Fraxineum, Symphytum Officinale, Hepar Suis, Lung (suis), Lymph Node (suis)
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Bioactive Nutritional, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
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:	ARCTIUM LAPPA ROOT - 4 [hp_X]/mL ARNICA MONTANA - 3 [hp_X]/mL ASCLEPIAS TUBEROSA ROOT - 4 [hp_X]/mL ATROPA BELLADONNA - 12 [hp_X]/mL BERBERIS VULGARIS ROOT BARK - 4 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP - 4 [hp_X]/mL CHELIDONIUM MAJUS - 4 [hp_X]/mL COMFREY ROOT - 6 [hp_X]/mL ECHINACEA ANGUSTIFOLIA - 4 [hp_X]/mL EUCALYPTUS GLOBULUS LEAF - 4 [hp_X]/mL Load more... FENUGREEK SEED - 4 [hp_X]/mL FRANGULA ALNUS BARK - 4 [hp_X]/mL FRANGULA PURSHIANA BARK - 4 [hp_X]/mL GLYCYRRHIZA GLABRA - 3 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE - 12 [hp_X]/mL MATRICARIA RECUTITA - 4 [hp_X]/mL NASTURTIUM OFFICINALE - 4 [hp_X]/mL NITRIC ACID - 12 [hp_X]/mL PHOSPHORIC ACID - 12 [hp_X]/mL PHYTOLACCA AMERICANA ROOT - 4 [hp_X]/mL PLANTAGO MAJOR - 3 [hp_X]/mL PORK LIVER - 8 [hp_X]/mL STILLINGIA SYLVATICA ROOT - 3 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED - 12 [hp_X]/mL SUS SCROFA LUNG - 8 [hp_X]/mL SUS SCROFA LYMPH - 8 [hp_X]/mL TARAXACUM OFFICINALE - 4 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER - 3 [hp_X]/mL URTICA DIOICA - 4 [hp_X]/mL ZANTHOXYLUM AMERICANUM BARK - 4 [hp_X]/mL
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
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:	16 Jun, 2017
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	09 May, 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:	BioActive Nutritional, 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.
NUI:	N0000185371 N0000185375 N0000175629 N0000184306 M0000728 M0006342 M0016962 N0000185001 M0516536
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	597E9BI3Z3 O80TY208ZW 1ZL82U5D18 WQZ3G9PF0H 1TH8Q20J0U 18E7415PXQ 7E889U5RNN M9VVZ08EKQ VB06AV5US8 S546YLW6E6 Load more... 654825W09Z S2D77IH61R 4VBP01X99F 2788Z9758H C88X29Y479 G0R4UBI2ZZ YH89GMV676 411VRN1TV4 E4GA8884NN 11E6VI8VEG W2469WNO6U 6EC706HI7F QBR70R4FBK 269XH13919 7GL3G1COB3 33A7VYU29L 39981FM375 4JS0838828 710FLW4U46 A4KL1HMZ7T
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:	Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant 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]
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] Dietary Proteins [CS] Plant Proteins [CS] Seed Storage 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] Cell-mediated Immunity [PE] Dietary Proteins [CS] Increased Histamine Release [PE] Increased IgG Production [PE] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Seed Storage 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
43857-0451-1	30 mL in 1 BOTTLE, DROPPER (43857-0451-1)	16 Jun, 2017	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

Industrotox

Glycyrrhiza Glabra & more..

Liquid
BioActive Nutritional, Inc.
NDC: 43857-0451

Purpose:

Homeopathic indications: for temporary relief of cough with sensation as if something were loose in the chest, rhinitis, hoarseness with rough, scraped feeling of the throat & stuffiness of the nose as a consequence of industrial pollutants.** **these statements are based upon homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Industrotox glycyrrhiza glabra, plantago major, stillingia sylvatica, trifolium pratense, arnica montana, asclepias tuberosa, berberis vulgaris, calendula officinalis, chamomilla, chelidonium majus, echinacea (angustifolia), eucalyptus globulus, lappa major, nasturtium aquaticum, phytolacca decandra, rhamnus frangula, rhamnus purshiana, taraxacum officinale, trigonella foenum-graecum, urtica dioica, xanthoxylum fraxineum, symphytum officinale, hepar suis, lung (suis), lymph node (suis) glycyrrhiza glabra glycyrrhiza glabra plantago major plantago major stillingia sylvatica root stillingia sylvatica root trifolium pratense flower trifolium pratense flower arnica montana arnica montana asclepias tuberosa root asclepias tuberosa root berberis vulgaris root bark berberis vulgaris root bark calendula officinalis flowering top calendula officinalis flowering top matricaria recutita matricaria chamomilla chelidonium majus chelidonium majus echinacea angustifolia echinacea angustifolia eucalyptus globulus leaf eucalyptus globulus leaf arctium lappa root arctium lappa root nasturtium officinale nasturtium officinale phytolacca americana root phytolacca americana root frangula alnus bark frangula alnus bark frangula purshiana bark frangula purshiana bark taraxacum officinale taraxacum officinale fenugreek seed fenugreek seed urtica dioica urtica dioica zanthoxylum americanum bark zanthoxylum americanum bark comfrey root comfrey root pork liver pork liver sus scrofa lung sus scrofa lung sus scrofa lymph sus scrofa lymph atropa belladonna atropa belladonna lycopodium clavatum spore lycopodium clavatum spore nitric acid nitric acid strychnos nux-vomica seed strychnos nux-vomica seed phosphoric acid phosphoric acid water alcohol

Indications and Usage:

Warnings:

Warnings: if pregnant or breast-feeding, ask a health care professional before use. keep out of reach of children. in case of overdose, get medical help or contact a poison control center right away. do not use if tamper evident seal is broken or missing. store in a cool, dry place.

Dosage and Administration:

Directions: 10 drops orally, 3 times a day. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: bio active nutritional industrotox homeopathic 1 fl oz (30 ml) industrotox

Further Questions:

Questions: distributed by: bioactive nutritional, inc. 1803 n. wickham rd. melbourne, fl 32935

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.