Neurotransmitter Pro Liquid
NDC 44911-0710

View dosage, usage, ingredients, routes, and UNII mappings.
Table of Contents
  1. Product Information
  2. Product Packages
  3. What is NDC 44911-0710?
  4. Neurotransmitter Pro Uses
  5. Active Ingredients
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. Pharmacologic Classes

Product Information

Neurotransmitter Pro (aethusa cynapium, ginkgo biloba, kali phosphoricum, cerebrum suis, hypothalamus suis, adenosinum triphosphoricum dinatrum, alumina, anacardium orientale, arsenicum album, cortisone aceticum, levothyroxinum, lycopodium clavatum, nadidum, phosphorus, ubidecarenonum, zincum metallicum, acetylcholine chloride, dopamine hydrochloride, gaba (gamma-aminobutyric acid), histaminum hydrochloricum, melatonin, norepinephrine (bitartrate), serotonin (hydrochloride), oxytocin) is a UNAPPROVED HOMEOPATHIC-approved product labeled by Energique, Inc.. This medication is typically used as a catecholamine [epc]. It is supplied as a liquid for oral administration. This product entry covers the primary NDC 44911-0710 and its associated package configuration. This profile includes active and inactive ingredient UNII references and FDA labeling data.

Primary Identification

NDC Product Code:
44911-0710
Proprietary Name:
Neurotransmitter Pro
Non-Proprietary Name: [1]
Aethusa Cynapium, Ginkgo Biloba, Kali Phosphoricum, Cerebrum Suis, Hypothalamus Suis, Adenosinum Triphosphoricum Dinatrum, Alumina, Anacardium Orientale, Arsenicum Album, Cortisone Aceticum, Levothyroxinum, Lycopodium Clavatum, Nadidum, Phosphorus, Ubidecarenonum, Zincum Metallicum, Acetylcholine Chloride, Dopamine Hydrochloride, Gaba (gamma-aminobutyric Acid), Histaminum Hydrochloricum, Melatonin, Norepinephrine (bitartrate), Serotonin (hydrochloride), Oxytocin
Substance Name: [2]
.gamma.-aminobutyric Acid; Acetylcholine Chloride; Adenosine Triphosphate Disodium; Aethusa Cynapium Whole; Aluminum Oxide; Arsenic Trioxide; Cortisone Acetate; Dibasic Potassium Phosphate; Dopamine Hydrochloride; Ginkgo; Histamine Dihydrochloride; Levothyroxine; Lycopodium Clavatum Spore; Melatonin; Nadide; Norepinephrine Bitartrate; Oxytocin; Phosphorus; Semecarpus Anacardium Juice; Serotonin Hydrochloride; Sus Scrofa Cerebrum; Sus Scrofa Hypothalamus; Ubidecarenone; Zinc
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]
Energique, Inc.
Labeler Code:
44911
Product Label ID:
b433c635-e38b-4b3a-89cb-4a72a386ad84
Marketing Category: [8]
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.

Marketing Timeline

Start Marketing Date: [9]
05-06-2024
Listing Expiration Date: [11]
12-31-2026
Exclude Flag: [12]
N

Code Structure Chart

Product Details

What is NDC 44911-0710?

The NDC code 44911-0710 is assigned by the FDA to the product Neurotransmitter Pro. It is commonly known by its generic name, aethusa cynapium, ginkgo biloba, kali phosphoricum, cerebrum suis, hypothalamus suis, adenosinum triphosphoricum dinatrum, alumina, anacardium orientale, arsenicum album, cortisone aceticum, levothyroxinum, lycopodium clavatum, nadidum, phosphorus, ubidecarenonum, zincum metallicum, acetylcholine chloride, dopamine hydrochloride, gaba (gamma-aminobutyric acid), histaminum hydrochloricum, melatonin, norepinephrine (bitartrate), serotonin (hydrochloride), oxytocin. This pharmaceutical product is labeled by Energique, 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: 44911-0710-1. 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 and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional.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 30 [hp_X]/mL - The most common inhibitory neurotransmitter in the central nervous system.
  • ACETYLCHOLINE CHLORIDE 30 [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.
  • ADENOSINE TRIPHOSPHATE DISODIUM 12 [hp_X]/mL
  • AETHUSA CYNAPIUM WHOLE 6 [hp_X]/mL
  • ALUMINUM OXIDE 12 [hp_X]/mL - An oxide of aluminum, occurring in nature as various minerals such as bauxite, corundum, etc. It is used as an adsorbent, desiccating agent, and catalyst, and in the manufacture of dental cements and refractories.
  • ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
  • CORTISONE ACETATE 12 [hp_X]/mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
  • DIBASIC POTASSIUM PHOSPHATE 6 [hp_X]/mL
  • DOPAMINE HYDROCHLORIDE 30 [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.
  • GINKGO 6 [hp_X]/mL - The only specie of the genus Ginkgo, family Ginkgoacea. It is the source of extracts of medicinal interest, especially Egb 761. Ginkgo may refer to the genus or species.
  • HISTAMINE DIHYDROCHLORIDE 30 [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.
  • LEVOTHYROXINE 12 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 12 [hp_X]/mL
  • MELATONIN 30 [hp_X]/mL - A biogenic amine that is found in animals and plants. In mammals, melatonin is produced by the PINEAL GLAND. Its secretion increases in darkness and decreases during exposure to light. Melatonin is implicated in the regulation of SLEEP, mood, and REPRODUCTION. Melatonin is also an effective antioxidant.
  • NADIDE 12 [hp_X]/mL
  • NOREPINEPHRINE BITARTRATE 30 [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.
  • OXYTOCIN 36 [hp_C]/mL - A nonapeptide hormone released from the neurohypophysis (PITUITARY GLAND, POSTERIOR). It differs from VASOPRESSIN by two amino acids at residues 3 and 8. Oxytocin acts on SMOOTH MUSCLE CELLS, such as causing UTERINE CONTRACTIONS and MILK EJECTION.
  • PHOSPHORUS 12 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
  • SEMECARPUS ANACARDIUM JUICE 12 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 30 [hp_X]/mL
  • SUS SCROFA CEREBRUM 8 [hp_X]/mL
  • SUS SCROFA HYPOTHALAMUS 8 [hp_X]/mL
  • UBIDECARENONE 12 [hp_X]/mL
  • ZINC 12 [hp_X]/mL - A metallic element of atomic number 30 and atomic weight 65.38. It is a necessary trace element in the diet, forming an essential part of many enzymes, and playing an important role in protein synthesis and in cell division. Zinc deficiency is associated with ANEMIA, short stature, HYPOGONADISM, impaired WOUND HEALING, and geophagia. It is known by the symbol Zn.

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".