Bio Cytotox Phase Liquid
NDC 43742-1493

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1493?
  4. Bio Cytotox Phase Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Bio Cytotox Phase (podophyllum peltatum, ascorbicum acidum, galium aparine, hydrastis canadensis, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, sarcolacticum acidum, thiaminum hydrochloricum, alpha-lipoicum acidum, colchicum autumnale, conium maculatum, natrum oxalaceticum, sulphur, vaccinium myrtillus, norepinephrine, acetylsalicylicum acidum, adenosinum triphosphoricum dinatrum, anthrachinonum, histaminum hydrochloricum, magnesium gluconicum dihydricum, nadidum, naphthochinonum, pantothenic acid, ubidecarenonum,) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Deseret Biologicals, Inc.. This medication is typically used as a analogs/derivatives [chemical/ingredient]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 43742-1493 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
43742-1493
Proprietary Name:
Bio Cytotox Phase
Non-Proprietary Name: [1]
Podophyllum Peltatum, Ascorbicum Acidum, Galium Aparine, Hydrastis Canadensis, Nicotinamidum, Pyridoxinum Hydrochloricum, Riboflavinum, Sarcolacticum Acidum, Thiaminum Hydrochloricum, Alpha-lipoicum Acidum, Colchicum Autumnale, Conium Maculatum, Natrum Oxalaceticum, Sulphur, Vaccinium Myrtillus, Norepinephrine, Acetylsalicylicum Acidum, Adenosinum Triphosphoricum Dinatrum, Anthrachinonum, Histaminum Hydrochloricum, Magnesium Gluconicum Dihydricum, Nadidum, Naphthochinonum, Pantothenic Acid, Ubidecarenonum,
Substance Name: [2]
Adenosine Triphosphate Disodium; Anthraquinone; Ascorbic Acid; Aspirin; Bilberry; Colchicum Autumnale Bulb; Conium Maculatum Flowering Top; Galium Aparine; Goldenseal; Histamine Dihydrochloride; Hydroquinone; Lactic Acid, L-; Magnesium Gluconate; Manganese Phosphate, Dibasic; Nadide; Naphthoquine; Niacinamide; Norepinephrine Bitartrate; Pantothenic Acid; Podophyllum; Pyridoxine Hydrochloride; Riboflavin; Salmonella Enterica Subsp. Enterica Serovar Enteritidis; Sodium Diethyl Oxalacetate; Sulfur; Thiamine Hydrochloride; Thioctic Acid; Ubidecarenone
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]
Deseret Biologicals, Inc.
Labeler Code:
43742
Product Label ID:
ca632470-6cbc-4994-a7f0-95b6ad9aa44f
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
07-09-2019
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 43742-1493?

The NDC code 43742-1493 is assigned by the FDA to the product Bio Cytotox Phase. It is commonly known by its generic name, podophyllum peltatum, ascorbicum acidum, galium aparine, hydrastis canadensis, nicotinamidum, pyridoxinum hydrochloricum, riboflavinum, sarcolacticum acidum, thiaminum hydrochloricum, alpha-lipoicum acidum, colchicum autumnale, conium maculatum, natrum oxalaceticum, sulphur, vaccinium myrtillus, norepinephrine, acetylsalicylicum acidum, adenosinum triphosphoricum dinatrum, anthrachinonum, histaminum hydrochloricum, magnesium gluconicum dihydricum, nadidum, naphthochinonum, pantothenic acid, ubidecarenonum, . This pharmaceutical product is labeled by Deseret Biologicals, 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: 43742-1493-1. 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 the temporary relief of symptoms of fatigue, slowed metabolism, and weakened constitution.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms of fatigue, slowed metabolism, and weakened constitution.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

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.
  • ADENOSINE TRIPHOSPHATE DISODIUM 10 [hp_X]/mL
  • ANTHRAQUINONE 10 [hp_X]/mL - Compounds based on ANTHRACENES which contain two KETONES in any position. Substitutions can be in any position except on the ketone groups.
  • ASCORBIC ACID 6 [hp_X]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
  • ASPIRIN 10 [hp_X]/mL - The prototypical analgesic used in the treatment of mild to moderate pain. It has anti-inflammatory and antipyretic properties and acts as an inhibitor of cyclooxygenase which results in the inhibition of the biosynthesis of prostaglandins. Aspirin also inhibits platelet aggregation and is used in the prevention of arterial and venous thrombosis. (From Martindale, The Extra Pharmacopoeia, 30th ed, p5)
  • BILBERRY 8 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 8 [hp_X]/mL
  • CONIUM MACULATUM FLOWERING TOP 8 [hp_X]/mL
  • GALIUM APARINE 6 [hp_X]/mL - A genus of herbaceous annual and perennial plants in the family RUBIACEAE.
  • GOLDENSEAL 6 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 10 [hp_X]/mL - An amine derived by enzymatic decarboxylation of HISTIDINE. It is a powerful stimulant of gastric secretion, a constrictor of bronchial smooth muscle, a vasodilator, and also a centrally acting neurotransmitter.
  • HYDROQUINONE 3 [hp_C]/mL - Derivatives of hydroquinone (1,4-dihydrobenzene) made by reduction of BENZOQUINONES.
  • LACTIC ACID, L- 6 [hp_X]/mL
  • MAGNESIUM GLUCONATE 10 [hp_X]/mL
  • MANGANESE PHOSPHATE, DIBASIC 15 [hp_X]/mL
  • NADIDE 10 [hp_X]/mL
  • NAPHTHOQUINE 10 [hp_X]/mL - has antimalarial activity
  • NIACINAMIDE 6 [hp_X]/mL - An important compound functioning as a component of the coenzyme NAD. Its primary significance is in the prevention and/or cure of blacktongue and PELLAGRA. Most animals cannot manufacture this compound in amounts sufficient to prevent nutritional deficiency and it therefore must be supplemented through dietary intake.
  • NOREPINEPHRINE BITARTRATE 10 [hp_X]/mL - Precursor of epinephrine that is secreted by the ADRENAL MEDULLA and is a widespread central and autonomic neurotransmitter. Norepinephrine is the principal transmitter of most postganglionic sympathetic fibers, and of the diffuse projection system in the brain that arises from the LOCUS CERULEUS. It is also found in plants and is used pharmacologically as a sympathomimetic.
  • PANTOTHENIC ACID 10 [hp_X]/mL - A butyryl-beta-alanine that can also be viewed as pantoic acid complexed with BETA ALANINE. It is incorporated into COENZYME A and protects cells against peroxidative damage by increasing the level of GLUTATHIONE.
  • PODOPHYLLUM 5 [hp_X]/mL - A genus of poisonous American herbs, family BERBERIDACEAE. The roots yield PODOPHYLLOTOXIN and other pharmacologically important agents. The plant was formerly used as a cholagogue and cathartic. It is different from the European mandrake, MANDRAGORA.
  • PYRIDOXINE HYDROCHLORIDE 6 [hp_X]/mL - The 4-methanol form of VITAMIN B 6 which is converted to PYRIDOXAL PHOSPHATE which is a coenzyme for synthesis of amino acids, neurotransmitters (serotonin, norepinephrine), sphingolipids, aminolevulinic acid. Although pyridoxine and Vitamin B 6 are still frequently used as synonyms, especially by medical researchers, this practice is erroneous and sometimes misleading (EE Snell; Ann NY Acad Sci, vol 585 pg 1, 1990).
  • RIBOFLAVIN 6 [hp_X]/mL - Nutritional factor found in milk, eggs, malted barley, liver, kidney, heart, and leafy vegetables. The richest natural source is yeast. It occurs in the free form only in the retina of the eye, in whey, and in urine; its principal forms in tissues and cells are as FLAVIN MONONUCLEOTIDE and FLAVIN-ADENINE DINUCLEOTIDE.
  • SALMONELLA ENTERICA SUBSP. ENTERICA SEROVAR ENTERITIDIS 30 [hp_C]/mL
  • SODIUM DIETHYL OXALACETATE 8 [hp_X]/mL
  • SULFUR 8 [hp_X]/mL - An element that is a member of the chalcogen family. It has an atomic symbol S, atomic number 16, and atomic weight [32.059; 32.076]. It is found in the amino acids cysteine and methionine.
  • THIAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • THIOCTIC ACID 8 [hp_X]/mL - An octanoic acid bridged with two sulfurs so that it is sometimes also called a pentanoic acid in some naming schemes. It is biosynthesized by cleavage of LINOLEIC ACID and is a coenzyme of oxoglutarate dehydrogenase (KETOGLUTARATE DEHYDROGENASE COMPLEX). It is used in DIETARY SUPPLEMENTS.
  • UBIDECARENONE 10 [hp_X]/mL

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".