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  4. NDC Product Code: 43742-1647 Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate)

NDC 43742-1647 Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate)

Liquid - View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. What is NDC 43742-1647?
  4. Active Ingredients

Product Information

This product is an UNFINISHED DRUG part of the official NDC directory. Unfinished drugs include products like active ingredients some of which are used in bulk for further processing or compounding. The FDA requires a list of these drugs manufactured in a U.S. commercial distribution facility.
NDC Product Code:
43742-1647
Proprietary Name:
Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate)
Non-Proprietary Name: [1]
Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate)
Substance Name: [2]
.gamma.-aminobutyric Acid; Acetaldehyde; Acetylcholine Chloride; Black Cohosh; Cholesterol; Dopamine Hydrochloride; Epinephrine; Eugenol; Gelsemium Sempervirens Root; Goldenseal; Histamine Dihydrochloride; Norepinephrine Bitartrate; Phenyl Isothiocyanate; Phenylalanine; Progesterone; Taraxacum Officinale; Taurine; Toxicodendron Pubescens Leaf; Tyramine
NDC Directory Status:
Bulk Ingredient
Product Type: [3]
UNFINISHED PRODUCT INCLUDED in the NDC Directory
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.
Labeler Name: [5]
Deseret Biologicals, Inc.
Labeler Code:
43742
Marketing Category: [8]
DRUG FOR FURTHER PROCESSING - A drug (other than the bulk ingredient API) that is in an interim stage of manufacture, processing, preparation, or packaging, and not ready for human or animal use.
Start Marketing Date: [9]
05-22-2020
End Marketing Date: [10]
06-02-2025
Exclude Flag: [12]
N
Unfinished Product: [13]
Yes
Code Navigator:

Code Structure Chart

Product Details

What is NDC 43742-1647?

The NDC code 43742-1647 is assigned by the FDA to the UNFINISHED product Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate) which is a bulk ingredient product labeled by Deseret Biologicals, Inc.. The generic name of Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate) is hydrastis canadensis, taraxacum officinale, cimicifuga racemosa, gelsemium sempervirens, rhus tox, acetaldehyde, cholesterinum, dopamine hydrochloride, eugenol, l-phenylalanine, phenyl isothiocyanate, progesterone, taurine, tyramine, acetylcholine chloride, adrenalinum, gaba, histaminum hydrochloricum, norepinephrine (bitartrate). The product's dosage form is liquid. The product is distributed in a single package with assigned NDC code 43742-1647-1 960 ml in 1 bottle . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are Hydrastis Canadensis, Taraxacum Officinale, Cimicifuga Racemosa, Gelsemium Sempervirens, Rhus Tox, Acetaldehyde, Cholesterinum, Dopamine Hydrochloride, Eugenol, L-phenylalanine, Phenyl Isothiocyanate, Progesterone, Taurine, Tyramine, Acetylcholine Chloride, Adrenalinum, Gaba, Histaminum Hydrochloricum, Norepinephrine (bitartrate) Active Ingredients?

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.
  • .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]/mL - The most common inhibitory neurotransmitter in the central nervous system.
  • ACETALDEHYDE 6 [hp_X]/mL - A colorless, flammable liquid used in the manufacture of acetic acid, perfumes, and flavors. It is also an intermediate in the metabolism of alcohol. It has a general narcotic action and also causes irritation of mucous membranes. Large doses may cause death from respiratory paralysis.
  • ACETYLCHOLINE CHLORIDE 6 [hp_X]/mL - A neurotransmitter found at neuromuscular junctions, autonomic ganglia, parasympathetic effector junctions, a subset of sympathetic effector junctions, and at many sites in the central nervous system.
  • BLACK COHOSH 6 [hp_X]/mL
  • CHOLESTEROL 6 [hp_X]/mL - The principal sterol of all higher animals, distributed in body tissues, especially the brain and spinal cord, and in animal fats and oils.
  • DOPAMINE HYDROCHLORIDE 6 [hp_X]/mL - One of the catecholamine NEUROTRANSMITTERS in the brain. It is derived from TYROSINE and is the precursor to NOREPINEPHRINE and EPINEPHRINE. Dopamine is a major transmitter in the extrapyramidal system of the brain, and important in regulating movement. A family of receptors (RECEPTORS, DOPAMINE) mediate its action.
  • EPINEPHRINE 6 [hp_X]/mL - The active sympathomimetic hormone from the ADRENAL MEDULLA. It stimulates both the alpha- and beta- adrenergic systems, causes systemic VASOCONSTRICTION and gastrointestinal relaxation, stimulates the HEART, and dilates BRONCHI and cerebral vessels. It is used in ASTHMA and CARDIAC FAILURE and to delay absorption of local ANESTHETICS.
  • EUGENOL 6 [hp_X]/mL - A cinnamate derivative of the shikimate pathway found in CLOVE OIL and other PLANTS.
  • GELSEMIUM SEMPERVIRENS ROOT 6 [hp_X]/mL
  • GOLDENSEAL 6 [hp_X]/mL
  • HISTAMINE DIHYDROCHLORIDE 6 [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.
  • NOREPINEPHRINE BITARTRATE 6 [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.
  • PHENYL ISOTHIOCYANATE 6 [hp_X]/mL
  • PHENYLALANINE 6 [hp_X]/mL - An essential aromatic amino acid that is a precursor of MELANIN; DOPAMINE; noradrenalin (NOREPINEPHRINE), and THYROXINE.
  • PROGESTERONE 6 [hp_X]/mL - The major progestational steroid that is secreted primarily by the CORPUS LUTEUM and the PLACENTA. Progesterone acts on the UTERUS, the MAMMARY GLANDS and the BRAIN. It is required in EMBRYO IMPLANTATION; PREGNANCY maintenance, and the development of mammary tissue for MILK production. Progesterone, converted from PREGNENOLONE, also serves as an intermediate in the biosynthesis of GONADAL STEROID HORMONES and adrenal CORTICOSTEROIDS.
  • TARAXACUM OFFICINALE 6 [hp_X]/mL - A plant genus of the family Asteraceae. Members contain chicoric and chlorogenic acids and germacrane- and eudesmane-type SESQUITERPENES.
  • TAURINE 6 [hp_X]/mL - A conditionally essential nutrient, important during mammalian development. It is present in milk but is isolated mostly from ox bile and strongly conjugates bile acids.
  • TOXICODENDRON PUBESCENS LEAF 6 [hp_X]/mL
  • TYRAMINE 6 [hp_X]/mL - An indirect sympathomimetic that occurs naturally in cheese and other foods. Tyramine does not directly activate adrenergic receptors, but it can serve as a substrate for adrenergic uptake systems and MONOAMINE OXIDASE to prolong the actions of adrenergic transmitters. It also provokes transmitter release from adrenergic terminals and may be a neurotransmitter in some invertebrate nervous systems.

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Product Footnotes

[1] 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.

[2] 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.

[3] 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.

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

[8] 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.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[10] 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.

[12] 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 ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".

[13] What is an Unfinished Product? - This field indicates if the product is an unfinished drug. An unfinished drug is an active pharmaceutical ingredient either alone or with other ingredients that is not a finished drug product. Unfinished drugs are used to process other drugs or for drug compounding.