Hepatatox Liquid
NDC 43857-0543

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43857-0543?
  4. Hepatatox Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Hepatatox (triticum aestivum, chelidonium majus, taraxacum officinale, glutathione, hepar suis, thyroidinum (suis), lycopodium clavatum, nux vomica, phosphoricum acidum, adrenocorticotrophin, salicylicum acidum, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum, chlorinum potassium sorbate, sorbitol, resorcinum, benzyl alcohol, lacticum acidum, isopropyl palmitate, boricum acidum, aceticum acidum, phenyl butazone, petroleum jelly, plumbum metallicum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Bioactive Nutritional, Inc. This medication is typically used as a adrenocorticotropic hormone [cs]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43857-0543 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43857-0543
Proprietary Name:
Hepatatox
Non-Proprietary Name: [1]
Triticum Aestivum, Chelidonium Majus, Taraxacum Officinale, Glutathione, Hepar Suis, Thyroidinum (suis), Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Adrenocorticotrophin, Salicylicum Acidum, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum, Chlorinum Potassium Sorbate, Sorbitol, Resorcinum, Benzyl Alcohol, Lacticum Acidum, Isopropyl Palmitate, Boricum Acidum, Aceticum Acidum, Phenyl Butazone, Petroleum Jelly, Plumbum Metallicum
Substance Name: [2]
Triticum Aestivum Whole; Chelidonium Majus Whole; Taraxacum Officinale; Glutathione; Pork Liver; Thyroid; Lycopodium Clavatum Spore; Strychnos Nux-vomica Seed; Phosphoric Acid; Corticotropin; Salicylic Acid; Cortisone Acetate; Eugenol; Stearyl Alcohol; Xylitol; Estrone; Benzoic Acid; Chlorine; Potassium Sorbate; Sorbitol; Resorcinol; Benzyl Alcohol; Lactic Acid, Dl-; Isopropyl Palmitate; Boric Acid; Acetic Acid; Phenylbutazone; Petrolatum; Lead
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE PRODUCT INCLUDED in the NDC Directory
Code Navigator:

Clinical Specifications

Dosage Form:
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route(s): [4]
Oral - Administration to or by way of the mouth.

Labeler & Regulatory Data

Labeler Name: [5]
Bioactive Nutritional, Inc
Labeler Code:
43857
Product Label ID:
a113a9f1-4792-41a5-8d1b-a6756f356e15
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
02-20-2020
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43857-0543?

The NDC code 43857-0543 is assigned by the FDA to the product Hepatatox. It is commonly known by its generic name, triticum aestivum, chelidonium majus, taraxacum officinale, glutathione, hepar suis, thyroidinum (suis), lycopodium clavatum, nux vomica, phosphoricum acidum, adrenocorticotrophin, salicylicum acidum, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum, chlorinum potassium sorbate, sorbitol, resorcinum, benzyl alcohol, lacticum acidum, isopropyl palmitate, boricum acidum, aceticum acidum, phenyl butazone, petroleum jelly, plumbum metallicum. This pharmaceutical product is labeled by Bioactive Nutritional, Inc and is currently categorized as listed product. The medication is a liquid administered via oral route. In terms of distribution, this product is available in a single package configuration. The associated package NDC(s) include: 43857-0543-1. Beyond standard identification, this entry provides technical data including pharmacologic classes, UNII ingredient references, and RxNorm cross-referencing for healthcare systems.

What are the uses of this product?

For temporary relief of dyspepsia, flatulence, exhaustion, and nausea as a consequence of constipation. For temporary relief of dyspepsia, flatulence, exhaustion, and nausea as a consequence of constipation.

What are Active Ingredients of this product?

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.
  • TRITICUM AESTIVUM WHOLE 30 [hp_X]/mL
  • CHELIDONIUM MAJUS WHOLE 30 [hp_X]/mL
  • TARAXACUM OFFICINALE 30 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
  • GLUTATHIONE 30 [hp_X]/mL - A tripeptide with many roles in cells. It conjugates to drugs to make them more soluble for excretion, is a cofactor for some enzymes, is involved in protein disulfide bond rearrangement and reduces peroxides.
  • PORK LIVER 3 [hp_X]/mL
  • THYROID 30 [hp_X]/mL - A highly vascularized endocrine gland consisting of two lobes joined by a thin band of tissue with one lobe on each side of the TRACHEA. It secretes THYROID HORMONES from the follicular cells and CALCITONIN from the parafollicular cells thereby regulating METABOLISM and CALCIUM level in blood, respectively.
  • LYCOPODIUM CLAVATUM SPORE 30 [hp_C]/mL
  • STRYCHNOS NUX-VOMICA SEED 30 [hp_X]/mL
  • PHOSPHORIC ACID 30 [hp_X]/mL - Inorganic derivatives of phosphoric acid (H3PO4). Note that organic derivatives of phosphoric acids are listed under ORGANOPHOSPHATES.
  • CORTICOTROPIN 30 [hp_X]/mL
  • SALICYLIC ACID 6 [hp_X]/mL - A compound obtained from the bark of the white willow and wintergreen leaves. It has bacteriostatic, fungicidal, and keratolytic actions.
  • CORTISONE ACETATE 30 [hp_X]/mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
  • EUGENOL 30 [hp_X]/mL - A cinnamate derivative of the shikimate pathway found in CLOVE OIL and other PLANTS.
  • STEARYL ALCOHOL 30 [hp_X]/mL
  • XYLITOL 12 [hp_X]/mL - A five-carbon sugar alcohol derived from XYLOSE by reduction of the carbonyl group. It is as sweet as sucrose and used as a noncariogenic sweetener.
  • ESTRONE 30 [hp_X]/mL - An aromatized C18 steroid with a 3-hydroxyl group and a 17-ketone, a major mammalian estrogen. It is converted from ANDROSTENEDIONE directly, or from TESTOSTERONE via ESTRADIOL. In humans, it is produced primarily by the cyclic ovaries, PLACENTA, and the ADIPOSE TISSUE of men and postmenopausal women.
  • BENZOIC ACID 30 [hp_X]/mL - A fungistatic compound that is widely used as a food preservative. It is conjugated to GLYCINE in the liver and excreted as hippuric acid.
  • CHLORINE 12 [hp_X]/mL - An element with atomic symbol Cl, atomic number 17, and atomic weight 35, and member of the halogen family.
  • POTASSIUM SORBATE 8 [hp_X]/mL - Mold and yeast inhibitor. Used as a fungistatic agent for foods, especially cheeses.
  • SORBITOL 30 [hp_X]/mL - A polyhydric alcohol with about half the sweetness of sucrose. Sorbitol occurs naturally and is also produced synthetically from glucose. It was formerly used as a diuretic and may still be used as a laxative and in irrigating solutions for some surgical procedures. It is also used in many manufacturing processes, as a pharmaceutical aid, and in several research applications.
  • RESORCINOL 30 [hp_X]/mL - A water-soluble crystalline benzene-1,3-diol (resorcinol) and its derivatives.
  • BENZYL ALCOHOL 30 [hp_X]/mL - Alcohols derived from the aryl radical (C6H5CH2-) and defined by C6H5CHOH. The concept includes derivatives with any substituents on the benzene ring.
  • LACTIC ACID, DL- 30 [hp_X]/mL
  • ISOPROPYL PALMITATE 30 [hp_X]/mL
  • BORIC ACID 12 [hp_X]/mL - Inorganic and organic derivatives of boric acid either B(OH)3 or, preferably H3BO3.
  • ACETIC ACID 3 [hp_X]/mL - Product of the oxidation of ethanol and of the destructive distillation of wood. It is used locally, occasionally internally, as a counterirritant and also as a reagent. (Stedman, 26th ed)
  • PHENYLBUTAZONE 8 [hp_X]/mL - A butyl-diphenyl-pyrazolidinedione that has anti-inflammatory, antipyretic, and analgesic activities. It has been used in ANKYLOSING SPONDYLITIS; RHEUMATOID ARTHRITIS; and REACTIVE ARTHRITIS.
  • PETROLATUM 1 [hp_X]/mL - A colloidal system of semisolid hydrocarbons obtained from PETROLEUM. It is used as an ointment base, topical protectant, and lubricant.
  • LEAD 30 [hp_X]/mL - A soft, grayish metal with poisonous salts; atomic number 82, atomic weight 207.2, symbol Pb.

Which are the associated UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are the Inactive Ingredients associated UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

Which are the Pharmacologic Classes of this product?

A pharmacologic class is a group of drugs that share the same scientifically documented properties. The following is a list of the reported pharmacologic class(es) corresponding to the active ingredients of this product.

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Product & Regulatory Definitions
What is the Non-Proprietary Name? The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
What is the Substance Name? 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.
What kind of product is this? 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.
What are the Administration Routes? The translation of the route code submitted by the firm, indicating route of administration.
What is the Labeler Name? Name of Company corresponding to the labeler code segment of the Product NDC.
What is the Marketing Category? 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.
What is the Start Marketing Date? This is the date that the labeler indicates was the start of its marketing of the drug product.
What is the Listing Expiration Date? This is the date when the listing record will expire if not updated or certified by the product labeler.
What is the NDC Exclude Flag? This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions, or because the listing certification is expired, or because the listing data was inactivated by FDA, or because it was discontinued by the labeler. Possible values in this field are: "D", "E", "I", "N", "U".