NDC 62185-0042 Brain Support

Acetylcholine Chloride,Octopamine,Taurine,Adenosinum Cyclophosphoricum,Cerebrum - View Dosage, Usage, Ingredients, Routes, UNII

Product Information

NDC Product Code:
62185-0042
Proprietary Name:
Brain Support
Non-Proprietary Name: [1]
Acetylcholine Chloride, Octopamine, Taurine, Adenosinum Cyclophosphoricum, Cerebrum (suis), Diencephalon (suis), Pineal Gland (suis), Thalamus Opticus (suis), Adrenalinum, Dopamine Hydrochloride, Gaba (gamma-aminobutyric Acid), Norepinephrine (bitartrate), Serotonin (hydrochloride)
Substance Name: [2]
.gamma.-aminobutyric Acid; Acetylcholine Chloride; Adenosine Cyclic Phosphate; Dopamine Hydrochloride; Epinephrine; Norepinephrine Bitartrate; Octopamine; Serotonin Hydrochloride; Sus Scrofa Cerebrum; Sus Scrofa Diencephalon; Sus Scrofa Pineal Gland; Sus Scrofa Thalamus Lateral Geniculate Nucleus; Taurine
NDC Directory Status:
Human Otc Drug
Product Type: [3]
ACTIVE 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.
Administration Route(s): [4]
  • Oral - Administration to or by way of the mouth.
  • Labeler Name: [5]
    Dr. Donna Restivo Dc
    Labeler Code:
    62185
    Marketing Category: [8]
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date: [9]
    03-15-2019
    End Marketing Date: [10]
    04-15-2024
    Exclude Flag: [12]
    N
    Code Structure:
    Code Navigator:

    Product Packages

    NDC Code 62185-0042-1

    Package Description: 30 mL in 1 BOTTLE, DROPPER

    Product Details

    What is NDC 62185-0042?

    The NDC code 62185-0042 is assigned by the FDA to the product Brain Support which is a human over the counter drug product labeled by Dr. Donna Restivo Dc. The generic name of Brain Support is acetylcholine chloride, octopamine, taurine, adenosinum cyclophosphoricum, cerebrum (suis), diencephalon (suis), pineal gland (suis), thalamus opticus (suis), adrenalinum, dopamine hydrochloride, gaba (gamma-aminobutyric acid), norepinephrine (bitartrate), serotonin (hydrochloride). The product's dosage form is liquid and is administered via oral form. The product is distributed in a single package with assigned NDC code 62185-0042-1 30 ml in 1 bottle, dropper . 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 the uses for Brain Support?

    For temporary relief of symptoms related to sleep, memory, and emotional issues.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For temporary relief of symptoms related to sleep, memory, and emotional issues.****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration.

    What are Brain Support 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 8 [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.
    • ADENOSINE CYCLIC PHOSPHATE 8 [hp_X]/mL
    • DOPAMINE HYDROCHLORIDE 8 [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 8 [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.
    • NOREPINEPHRINE BITARTRATE 8 [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.
    • OCTOPAMINE 6 [hp_X]/mL - An alpha-adrenergic sympathomimetic amine, biosynthesized from tyramine in the CNS and platelets and also in invertebrate nervous systems. It is used to treat hypotension and as a cardiotonic. The natural D(-) form is more potent than the L(+) form in producing cardiovascular adrenergic responses. It is also a neurotransmitter in some invertebrates.
    • SEROTONIN HYDROCHLORIDE 8 [hp_X]/mL
    • SUS SCROFA CEREBRUM 8 [hp_X]/mL
    • SUS SCROFA DIENCEPHALON 8 [hp_X]/mL
    • SUS SCROFA PINEAL GLAND 8 [hp_X]/mL
    • SUS SCROFA THALAMUS LATERAL GENICULATE NUCLEUS 8 [hp_X]/mL
    • 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.

    Which are Brain Support UNII Codes?

    The UNII codes for the active ingredients in this product are:

    Which are Brain Support 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:

    * Please review the disclaimer below.

    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.

    [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.

    [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".