43857-0451 NDC - 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))

Drug Information

Product NDC: 43857-0451

Proprietary Name: Industrotox

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)

Active Ingredient(s):
  • 4 [hp_X]/mL ARCTIUM LAPPA ROOT;
  • 3 [hp_X]/mL ARNICA MONTANA;
  • 4 [hp_X]/mL ASCLEPIAS TUBEROSA ROOT;
  • 12 [hp_X]/mL ATROPA BELLADONNA;
  • 4 [hp_X]/mL BERBERIS VULGARIS ROOT BARK;
  • 4 [hp_X]/mL CALENDULA OFFICINALIS FLOWERING TOP;
  • 4 [hp_X]/mL CHELIDONIUM MAJUS;
  • 6 [hp_X]/mL COMFREY ROOT;
  • 4 [hp_X]/mL ECHINACEA ANGUSTIFOLIA;
  • 4 [hp_X]/mL EUCALYPTUS GLOBULUS LEAF;
  • 4 [hp_X]/mL FENUGREEK SEED;
  • 4 [hp_X]/mL FRANGULA ALNUS BARK;
  • 4 [hp_X]/mL FRANGULA PURSHIANA BARK;
  • 3 [hp_X]/mL GLYCYRRHIZA GLABRA;
  • 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 4 [hp_X]/mL MATRICARIA RECUTITA;
  • 4 [hp_X]/mL NASTURTIUM OFFICINALE;
  • 12 [hp_X]/mL NITRIC ACID;
  • 12 [hp_X]/mL PHOSPHORIC ACID;
  • 4 [hp_X]/mL PHYTOLACCA AMERICANA ROOT;
  • 3 [hp_X]/mL PLANTAGO MAJOR;
  • 8 [hp_X]/mL PORK LIVER;
  • 3 [hp_X]/mL STILLINGIA SYLVATICA ROOT;
  • 12 [hp_X]/mL STRYCHNOS NUX-VOMICA SEED;
  • 8 [hp_X]/mL SUS SCROFA LUNG;
  • 8 [hp_X]/mL SUS SCROFA LYMPH;
  • 4 [hp_X]/mL TARAXACUM OFFICINALE;
  • 3 [hp_X]/mL TRIFOLIUM PRATENSE FLOWER;
  • 4 [hp_X]/mL URTICA DIOICA;
  • 4 [hp_X]/mL ZANTHOXYLUM AMERICANUM BARK


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased IgG Production [PE];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Non-Standardized Plant Allergenic Extract [EPC];
  • Plant Proteins [CS];
  • Plant Proteins [CS];
  • Seed Storage Proteins [CS]

Labeler Information

Labeler Name: BioActive Nutritional, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:6/16/2017

Package Information

No. Package Code Package Description Billing Unit
143857-0451-130 mL in 1 BOTTLE, DROPPER (43857-0451-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43857-0451The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEIndustrotoxThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEGlycyrrhiza 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)The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE6/16/2017This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEBioActive Nutritional, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEARCTIUM LAPPA ROOT; ARNICA MONTANA; ASCLEPIAS TUBEROSA ROOT; ATROPA BELLADONNA; BERBERIS VULGARIS ROOT BARK; CALENDULA OFFICINALIS FLOWERING TOP; CHELIDONIUM MAJUS; COMFREY ROOT; ECHINACEA ANGUSTIFOLIA; EUCALYPTUS GLOBULUS LEAF; FENUGREEK SEED; FRANGULA ALNUS BARK; FRANGULA PURSHIANA BARK; GLYCYRRHIZA GLABRA; LYCOPODIUM CLAVATUM SPORE; MATRICARIA RECUTITA; NASTURTIUM OFFICINALE; NITRIC ACID; PHOSPHORIC ACID; PHYTOLACCA AMERICANA ROOT; PLANTAGO MAJOR; PORK LIVER; STILLINGIA SYLVATICA ROOT; STRYCHNOS NUX-VOMICA SEED; SUS SCROFA LUNG; SUS SCROFA LYMPH; TARAXACUM OFFICINALE; TRIFOLIUM PRATENSE FLOWER; URTICA DIOICA; ZANTHOXYLUM AMERICANUM BARKAn 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.
ACTIVE NUMERATOR STRENGTH4; 3; 4; 12; 4; 4; 4; 6; 4; 4; 4; 4; 4; 3; 12; 4; 4; 12; 12; 4; 3; 8; 3; 12; 8; 8; 4; 3; 4; 4 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS], Plant Proteins [CS], Seed Storage Proteins [CS] 

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This page was last updated on: 2/1/2023