NDC 50181-0041 Neurobalance Pro
Adrenocorticotrophin,Gaba,Glutamic Acid,Norepinephrine,Acetylcholine - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 50181 - The Wellness Center For Reseach And Education, Inc.
- 50181-0041 - Neurobalance Pro
Product Packages
NDC Code 50181-0041-1
Package Description: 30 mL in 1 BOTTLE, SPRAY
Product Details
What is NDC 50181-0041?
What are the uses for Neurobalance Pro?
What are Neurobalance Pro Active Ingredients?
- .GAMMA.-AMINOBUTYRIC ACID 6 [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.
- BARIUM CARBONATE 6 [hp_C]/mL
- CORTICOTROPIN 6 [hp_X]/mL
- DATURA STRAMONIUM 30 [hp_C]/mL - A plant species of the genus DATURA, family SOLANACEAE, that contains TROPANES and other SOLANACEOUS ALKALOIDS.
- 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.
- GLUTAMIC ACID 6 [hp_X]/mL - A non-essential amino acid naturally occurring in the L-form. Glutamic acid is the most common excitatory neurotransmitter in the CENTRAL NERVOUS SYSTEM.
- LEVODOPA 6 [hp_X]/mL - The naturally occurring form of DIHYDROXYPHENYLALANINE and the immediate precursor of DOPAMINE. Unlike dopamine itself, it can be taken orally and crosses the blood-brain barrier. It is rapidly taken up by dopaminergic neurons and converted to DOPAMINE. It is used for the treatment of PARKINSONIAN DISORDERS and is usually given with agents that inhibit its conversion to dopamine outside of the central nervous system.
- NOREPINEPHRINE 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.
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_C]/mL
- SEMECARPUS ANACARDIUM JUICE 6 [hp_C]/mL
- SEROTONIN HYDROCHLORIDE 6 [hp_X]/mL
- THYROID, PORCINE 6 [hp_X]/mL
Which are Neurobalance Pro UNII Codes?
The UNII codes for the active ingredients in this product are:
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (Active Moiety)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I)
- .GAMMA.-AMINOBUTYRIC ACID (UNII: 2ACZ6IPC6I) (Active Moiety)
- GLUTAMIC ACID (UNII: 3KX376GY7L)
- GLUTAMIC ACID (UNII: 3KX376GY7L) (Active Moiety)
- NOREPINEPHRINE (UNII: X4W3ENH1CV)
- NOREPINEPHRINE (UNII: X4W3ENH1CV) (Active Moiety)
- ACETYLCHOLINE CHLORIDE (UNII: AF73293C2R)
- ACETYLCHOLINE (UNII: N9YNS0M02X) (Active Moiety)
- EPINEPHRINE (UNII: YKH834O4BH)
- EPINEPHRINE (UNII: YKH834O4BH) (Active Moiety)
- LEVODOPA (UNII: 46627O600J)
- LEVODOPA (UNII: 46627O600J) (Active Moiety)
- SEROTONIN HYDROCHLORIDE (UNII: GKN429M9VS)
- SEROTONIN (UNII: 333DO1RDJY) (Active Moiety)
- THYROID, PORCINE (UNII: 6RV024OAUQ)
- SUS SCROFA THYROID (UNII: 6RV024OAUQ) (Active Moiety)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU)
- SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (Active Moiety)
- BARIUM CARBONATE (UNII: 6P669D8HQ8)
- BARIUM CATION (UNII: V645272HLN) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3)
- DATURA STRAMONIUM (UNII: G6W4F0V8Z3) (Active Moiety)
Which are Neurobalance Pro Inactive Ingredients 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Neurobalance Pro?
- Adrenergic alpha-Agonists - [MoA] (Mechanism of Action)
- Adrenergic beta-Agonists - [MoA] (Mechanism of Action)
- Adrenocorticotropic Hormone - [CS]
- Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
- Amino Acids, Aromatic - [CS]
- Aromatic Amino Acid - [EPC] (Established Pharmacologic Class)
- Catecholamine - [EPC] (Established Pharmacologic Class)
- Catecholamines - [CS]
- Cholinergic Agonists - [MoA] (Mechanism of Action)
- Cholinergic Receptor Agonist - [EPC] (Established Pharmacologic Class)
- alpha-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
- beta-Adrenergic Agonist - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[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.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[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.
[11] 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.
[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".