NDC 43857-0049 Chemtox

Triticum Aestivum, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Xanthoxylum Fraxineum, Glandula Suprarenalis Suis, Hepar Suis, Lymph (suis), Thyroidinum (suis), Belladonna, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Salicylicum Acidum, Adrenocorticotrophin, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum

NDC Product Code 43857-0049

NDC Code: 43857-0049

Proprietary Name: Chemtox 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, Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Phytolacca Decandra, Rhamnus Frangula, Rhamnus Purshiana, Stillingia Sylvatica, Trifolium Pratense, Xanthoxylum Fraxineum, Glandula Suprarenalis Suis, Hepar Suis, Lymph (suis), Thyroidinum (suis), Belladonna, Lycopodium Clavatum, Nitricum Acidum, Nux Vomica, Phosphoricum Acidum, Phosphorus, Salicylicum Acidum, Adrenocorticotrophin, Cortisone Aceticum, Eugenol, Stearyl Alcohol, Xylitol, Folliculinum, Benzoicum Acidum 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.

NDC Code Structure

  • 43857 - Bioactive Nutritional, Inc.
    • 43857-0049 - Chemtox

NDC 43857-0049-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Chemtox with NDC 43857-0049 is a a human over the counter drug product labeled by Bioactive Nutritional, Inc.. The generic name of Chemtox is triticum aestivum, berberis vulgaris, glycyrrhiza glabra, lappa major, phytolacca decandra, rhamnus frangula, rhamnus purshiana, stillingia sylvatica, trifolium pratense, xanthoxylum fraxineum, glandula suprarenalis suis, hepar suis, lymph (suis), thyroidinum (suis), belladonna, lycopodium clavatum, nitricum acidum, nux vomica, phosphoricum acidum, phosphorus, salicylicum acidum, adrenocorticotrophin, cortisone aceticum, eugenol, stearyl alcohol, xylitol, folliculinum, benzoicum acidum. 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.

Chemtox 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
  • BERBERIS VULGARIS ROOT BARK 3 [hp_X]/mL
  • GLYCYRRHIZA GLABRA 3 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 3 [hp_X]/mL
  • PHYTOLACCA AMERICANA ROOT 3 [hp_X]/mL
  • FRANGULA ALNUS BARK 3 [hp_X]/mL
  • FRANGULA PURSHIANA BARK 3 [hp_X]/mL
  • STILLINGIA SYLVATICA ROOT 3 [hp_X]/mL
  • TRIFOLIUM PRATENSE FLOWER 3 [hp_X]/mL
  • ZANTHOXYLUM AMERICANUM BARK 3 [hp_X]/mL
  • SUS SCROFA ADRENAL GLAND 8 [hp_X]/mL
  • PORK LIVER 8 [hp_X]/mL
  • SUS SCROFA LYMPH 8 [hp_X]/mL
  • SUS SCROFA THYROID 8 [hp_X]/mL
  • ATROPA BELLADONNA WHOLE 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • NITRIC ACID 12 [hp_X]/mL
  • STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
  • PHOSPHORIC ACID 12 [hp_X]/mL
  • PHOSPHORUS 12 [hp_X]/mL
  • SALICYLIC ACID 30 [hp_X]/mL
  • CORTICOTROPIN 30 [hp_X]/mL
  • CORTISONE ACETATE 30 [hp_X]/mL
  • EUGENOL 30 [hp_X]/mL
  • STEARYL ALCOHOL 30 [hp_X]/mL
  • XYLITOL 30 [hp_X]/mL
  • ESTRONE 30 [hp_X]/mL
  • BENZOIC ACID 30 [hp_X]/mL
  • CHLORINE 30 [hp_X]/mL
  • POTASSIUM SORBATE 30 [hp_X]/mL
  • SORBITOL 30 [hp_X]/mL
  • RESORCINOL 30 [hp_X]/mL
  • BENZYL ALCOHOL 30 [hp_X]/mL
  • LACTIC ACID, DL- 30 [hp_X]/mL
  • ISOPROPYL PALMITATE 30 [hp_X]/mL
  • BORIC ACID 30 [hp_X]/mL
  • ACETIC ACID 30 [hp_X]/mL
  • PHENYLBUTAZONE 30 [hp_X]/mL
  • PETROLATUM 30 [hp_X]/mL
  • LEAD 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: 01-25-2013 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: 04-13-2022 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.

Chemtox Product Label Images

Chemtox 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 MT, Berberis Vulgaris 3X, Glycyrrhiza Glabra 3X, Lappa Major 3X, Phytolacca Decandra 3X, Rhamnus Frangula 3X, Rhamnus Purshiana 3X, Stillingia Sylvatica 3X, Trifolium Pratense 3X, Xanthoxylum Fraxineum 3X, Glandula Suprarenalis Suis 8X, Hepar Suis 8X, Lymph (suis) 8X, Thyroidinum (suis) 8X, Belladonna 12X, Lycopodium Clavatum 12X, Nitricum Acidum 12X, Nux Vomica 12X, Phosphoricum Acidum 12X, Phosphorus 12X, Salicylicum Acidum 30X, 60X, 200X, Adrenocorticotrophin 30X, 60X, 200X, Cortisone Aceticum 30X, 60X, 200X, Eugenol 30X, 60X, 200X, Stearyl Alcohol 30X, 60X, 200X, Xylitol 30X, 60X, 200X, Folliculinum 30X, 60X, 200X, Benzoicum Acidum 30X, 60X, 200X, Chlorinum 30X, 60X, 200X, Potassium Sorbate 30X, 60X, 200X, Sorbitol 30X, 60X, 200X, Resorcinum 30X, 60X, 200X, Benzyl Alcohol 30X, 60X, 200X, Lacticum Acidum 30X, 60X, 200X, Isopropyl Palmitate 30X, 60X, 200X, Boricum Acidum 30X, 60X, 200X, Aceticum Acidum 30X, 60X, 200X, Phenyl Butazone 30X, 60X, 200X, Petroleum Jelly 30X, 60X, 200X, Plumbum Metallicum 30X, 60X, 200X.Contains Wheat

Indications:

For temporary relief of weakness & exhaustion, minor abdominal cramps & bloating, and vomiting.

For temporary relief of weakness & exhaustion, minor abdominal cramps & bloating, and vomiting.

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.Contains Wheat

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:

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

Questions:

Distributed by:BioActive Nutritional, Inc.1803 N. Wickham Rd.Melbourne, FL 32935bioactivenutritional.com*For a complete list ofChemical Isodes contactBioActive Nutritional, Inc.

Package Label Display:

BIOActive NutritionalCHEMTOXHOMEOPATHIC1 FL OZ (30 ml)

* Please review the disclaimer below.

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