Neuro T Support Liquescence Liquid
NDC 83027-0032

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 83027-0032?
  4. Neuro T Support Liquescence Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Neuro T Support Liquescence (alfalfa, banana, valeriana officinalis, cholinum, gaba (gamma aminobutyric acid), inositol, oleander, hypophysis suis, hypothalamus suis, pineal gland (suis), scutellaria lateriflora, acetylcholine chloride, norepinephrine (bitartrate), cadmium metallicum, dopamine (hydrochloride), serotonin (hydrochloride), adrenalinum) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Nutritional Specialties, Inc.. This medication is typically used as a adrenergic alpha-agonists [moa]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 83027-0032 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
83027-0032
Proprietary Name:
Neuro T Support Liquescence
Non-Proprietary Name: [1]
Alfalfa, Banana, Valeriana Officinalis, Cholinum, Gaba (gamma Aminobutyric Acid), Inositol, Oleander, Hypophysis Suis, Hypothalamus Suis, Pineal Gland (suis), Scutellaria Lateriflora, Acetylcholine Chloride, Norepinephrine (bitartrate), Cadmium Metallicum, Dopamine (hydrochloride), Serotonin (hydrochloride), Adrenalinum
Substance Name: [2]
.gamma.-aminobutyric Acid; Acetylcholine Chloride; Banana; Cadmium; Choline Hydroxide; Dopamine Hydrochloride; Epinephrine; Inositol; Medicago Sativa Whole; Nerium Oleander Leaf; Norepinephrine Bitartrate; Scutellaria Lateriflora Whole; Serotonin Hydrochloride; Sus Scrofa Hypothalamus; Sus Scrofa Pineal Gland; Sus Scrofa Pituitary Gland; Valerian
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]
Nutritional Specialties, Inc.
Labeler Code:
83027
Product Label ID:
727f168a-6d9c-4ff5-b161-8bf0642a117b
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
04-25-2023
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 83027-0032?

The NDC code 83027-0032 is assigned by the FDA to the product Neuro T Support Liquescence. It is commonly known by its generic name, alfalfa, banana, valeriana officinalis, cholinum, gaba (gamma aminobutyric acid), inositol, oleander, hypophysis suis, hypothalamus suis, pineal gland (suis), scutellaria lateriflora, acetylcholine chloride, norepinephrine (bitartrate), cadmium metallicum, dopamine (hydrochloride), serotonin (hydrochloride), adrenalinum. This pharmaceutical product is labeled by Nutritional Specialties, 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: 83027-0032-1. 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?

Adults 1 to 2 teaspoons one to two times daily. Children under twelve one half adult dosage. Consult a physician for use in children under 12 years of age.

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.
  • .GAMMA.-AMINOBUTYRIC ACID 4 [hp_X]/mL - The most common inhibitory neurotransmitter in the central nervous system.
  • 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.
  • BANANA 3 [hp_X]/mL
  • CADMIUM 12 [hp_X]/mL - An element with atomic symbol Cd, atomic number 48, and atomic weight 112.41. It is a metal and ingestion will lead to CADMIUM POISONING.
  • CHOLINE HYDROXIDE 4 [hp_X]/mL - A basic constituent of lecithin that is found in many plants and animal organs. It is important as a precursor of acetylcholine, as a methyl donor in various metabolic processes, and in lipid metabolism.
  • DOPAMINE HYDROCHLORIDE 12 [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 12 [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.
  • INOSITOL 4 [hp_X]/mL - An isomer of glucose that has traditionally been considered to be a B vitamin although it has an uncertain status as a vitamin and a deficiency syndrome has not been identified in man. (From Martindale, The Extra Pharmacopoeia, 30th ed, p1379) Inositol phospholipids are important in signal transduction.
  • MEDICAGO SATIVA WHOLE 3 [hp_X]/mL
  • NERIUM OLEANDER LEAF 5 [hp_X]/mL
  • 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.
  • SCUTELLARIA LATERIFLORA WHOLE 6 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 12 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 6 [hp_X]/mL
  • SUS SCROFA PINEAL GLAND 6 [hp_X]/mL
  • SUS SCROFA PITUITARY GLAND 6 [hp_X]/mL
  • VALERIAN 3 [hp_X]/mL - A plant genus of the family VALERIANACEAE, order Dipsacales, subclass Asteridae, class Magnoliopsida. It is best known for the sedative use and valepotriate content of the roots. It is sometimes called Garden Heliotrope but is unrelated to true Heliotrope (HELIOTROPIUM).

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".