NDC 43857-0013 Hepatatox

Triticum Aestivum, Chelidonium Majus, Taraxacum Officinale, Glutathione, Hepar Suis, Thyroidinum (suis), Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Aceticum Acidum, Adrenocorticotrophin, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly, Phenylbutazone, Plumbum Metallicum, Potassium Sorbate, Resorcinol, Salicylieum Acidum, Sorbitol, Steary Alcohol, Xylitol,

NDC Product Code 43857-0013

NDC Code: 43857-0013

Proprietary Name: Hepatatox What is the Proprietary Name?
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: Triticum Aestivum, Chelidonium Majus, Taraxacum Officinale, Glutathione, Hepar Suis, Thyroidinum (suis), Lycopodium Clavatum, Nux Vomica, Phosphoricum Acidum, Aceticum Acidum, Adrenocorticotrophin, Benzoicum Acidum, Benzyl Alcohol, Boricum Acidum, Chlorinum, Cortisone Aceticum, Eugenol, Folliculinum, Isopropyl Palmitate, Lacticum Acidum, Petroleum Jelly, Phenylbutazone, Plumbum Metallicum, Potassium Sorbate, Resorcinol, Salicylieum Acidum, Sorbitol, Steary Alcohol, Xylitol, 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.


Code Structure
  • 43857 - Bioactive Nutritional, Inc.
    • 43857-0013 - Hepatatox

NDC 43857-0013-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Hepatatox with NDC 43857-0013 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Hepatatox is triticum aestivum, chelidonium majus, taraxacum officinale, glutathione, hepar suis, thyroidinum (suis), lycopodium clavatum, nux vomica, phosphoricum acidum, aceticum acidum, adrenocorticotrophin, benzoicum acidum, benzyl alcohol, boricum acidum, chlorinum, cortisone aceticum, eugenol, folliculinum, isopropyl palmitate, lacticum acidum, petroleum jelly, phenylbutazone, plumbum metallicum, potassium sorbate, resorcinol, salicylieum acidum, sorbitol, steary alcohol, xylitol,. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Bioactive Nutritional, Inc.

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.

Product Type: Human Otc Drug 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.


Hepatatox Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • TRITICUM AESTIVUM WHOLE 1 [hp_X]/mL
  • CHELIDONIUM MAJUS 3 [hp_X]/mL
  • TARAXACUM OFFICINALE 3 [hp_X]/mL
  • GLUTATHIONE 6 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • ACETIC ACID 30 [hp_X]/mL
  • CORTICOTROPIN 30 [hp_X]/mL
  • BENZOIC ACID 30 [hp_X]/mL
  • BENZYL ALCOHOL 30 [hp_X]/mL
  • BORIC ACID 30 [hp_X]/mL
  • CHLORINE 30 [hp_X]/mL
  • CORTISONE ACETATE 30 [hp_X]/mL
  • EUGENOL 30 [hp_X]/mL
  • ESTRONE 30 [hp_X]/mL
  • ISOPROPYL PALMITATE 30 [hp_X]/mL
  • LACTIC ACID, DL- 30 [hp_X]/mL
  • PETROLATUM 30 [hp_X]/mL
  • PHENYLBUTAZONE 30 [hp_X]/mL
  • LEAD 30 [hp_X]/mL
  • POTASSIUM SORBATE 30 [hp_X]/mL
  • RESORCINOL 30 [hp_X]/mL
  • SALICYLIC ACID 30 [hp_X]/mL
  • SORBITOL 30 [hp_X]/mL
  • STEARYL ALCOHOL 30 [hp_X]/mL
  • XYLITOL 30 [hp_X]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Bioactive Nutritional, Inc.
Labeler Code: 43857
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 01-17-2013 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 05-19-2019 What is the End Marketing Date?
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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Hepatatox Product Label Images

Hepatatox Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients

Triticum Aestivum 1X, Chelidonium Majus 3X, Taraxacum Officinale 3X, Glutathione 6X, Hepar Suis 8X, Thyroidinum (Suis) 8X, Lycopodium Clavatum 12X, Nux Vomica 12X, Phosphoricum Acidum 12X, Aceticum acidum 30X, 60X, 200X, Adrenocorticotrophin 30X, 60X, 200X, Benzoicum acidum 30X, 60X, 200X, Benzyl alcohol 30X, 60X, 200X, Boricum acidum 30X, 60X, 200X, Chlorinum 30X, 60X, 200X, Cortisone aceticum 30X, 60X, 200X, Eugenol 30X, 60X, 200X, Folliculinum 30X, 60X, 200X, Isopropyl palmitate 30X, 60X, 200X, Lacticum acidum 30X, 60X, 200X, Petroleum jelly 30X, 60X, 200X, Phenylbutazone 30X, 60X, 200X, Plumbum metallicum 30X, 60X, 200X, Potassium sorbate 30X, 60X, 200X, Resorcinol 30X, 60X, 200X, Salicylicum acidum 30X, 60X, 200X, Sorbitol 30X, 60X, 200X, Stearyl alcohol 30X, 60X, 200X, Xylitol 30X, 60X, 200X,

Indications

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

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 cool, dry place.

Directions

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

Inactive Ingredients

Demineralized water, 25% Ethanol.

Keep Out Of Reach Of Children

In case of overdose, get medical help or contact a Poison Control Center right away.

Indications And Usage

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

Questions

Distributed by:BIOACTIVE NUTRITIONALMelbourne, FL 32935For Nutritional Information write:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935

* Please review the disclaimer below.

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