43857-0531 NDC - EVTOX (COCHLEARIA OFFICINALIS, ECHINACEA (ANGUSTIFOLIA), HYDRASTIS CANADENSIS, LOMATIUM DISSECTUM, TABEBUIA IMPETIGINOSA, PROPOLIS, GLANDULA SUPRARENALIS SUIS, THYMUS (SUIS), ARANEA DIADEMA, IPECACUANHA, LYCOPODIUM CLAVATUM, MURIATICUM ACIDUM, NITRICUM ACIDUM, RHUS TOX, SILICEA, EPSTEIN-BARR VIRUS NOSODE)

Drug Information

Product NDC: 43857-0531
Proprietary Name: EVTOX
Non Proprietary Name: Cochlearia Officinalis, Echinacea (Angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Tabebuia Impetiginosa, Propolis, Glandula Suprarenalis Suis, Thymus (Suis), Aranea Diadema, Ipecacuanha, Lycopodium Clavatum, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Silicea, Epstein-Barr Virus Nosode
Active Ingredient(s): 12 [hp_X]/mL ARANEUS DIADEMATUS; 3 [hp_X]/mL COCHLEARIA OFFICINALIS FLOWERING TOP; 3 [hp_X]/mL ECHINACEA ANGUSTIFOLIA WHOLE; 5 [hp_X]/mL GOLDENSEAL; 30 [hp_C]/mL HUMAN HERPESVIRUS 4; 12 [hp_X]/mL HYDROCHLORIC ACID; 12 [hp_X]/mL IPECAC; 3 [hp_X]/mL LOMATIUM DISSECTUM ROOT; 12 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE; 12 [hp_X]/mL NITRIC ACID; 6 [hp_X]/mL PROPOLIS WAX; 12 [hp_X]/mL SILICON DIOXIDE; 8 [hp_X]/mL SUS SCROFA ADRENAL GLAND; 8 [hp_X]/mL SUS SCROFA THYMUS; 3 [hp_X]/mL TABEBUIA IMPETIGINOSA BARK; 12 [hp_X]/mL TOXICODENDRON PUBESCENS LEAF
Administration Route(s): ORAL
Dosage Form(s): LIQUID

Labeler Information

Field Name	Field Value
Labeler Name:	BioActive Nutritional, Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	10/3/2019

Package Information

No.	Package Code	Package Description	Billing Unit
1	43857-0531-1	30 mL in 1 BOTTLE, DROPPER (43857-0531-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	43857-0531	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.
PRODUCT TYPE NAME	HUMAN OTC DRUG	Indicates 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 NAME	EVTOX	The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAME	Cochlearia Officinalis, Echinacea (Angustifolia), Hydrastis Canadensis, Lomatium Dissectum, Tabebuia Impetiginosa, Propolis, Glandula Suprarenalis Suis, Thymus (Suis), Aranea Diadema, Ipecacuanha, Lycopodium Clavatum, Muriaticum Acidum, Nitricum Acidum, Rhus Tox, Silicea, Epstein-Barr Virus Nosode	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	LIQUID	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	10/3/2019	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	Product 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 NAME	BioActive Nutritional, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	ARANEUS DIADEMATUS; COCHLEARIA OFFICINALIS FLOWERING TOP; ECHINACEA ANGUSTIFOLIA WHOLE; GOLDENSEAL; HUMAN HERPESVIRUS 4; HYDROCHLORIC ACID; IPECAC; LOMATIUM DISSECTUM ROOT; LYCOPODIUM CLAVATUM SPORE; NITRIC ACID; PROPOLIS WAX; SILICON DIOXIDE; SUS SCROFA ADRENAL GLAND; SUS SCROFA THYMUS; TABEBUIA IMPETIGINOSA BARK; TOXICODENDRON PUBESCENS LEAF	An 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 STRENGTH	12; 3; 3; 5; 30; 12; 12; 3; 12; 12; 6; 12; 8; 8; 3; 12
ACTIVE INGRED UNIT	[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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

Drug Information

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