NDC 62185-0011 Brain Support

Acetylcholine Chloride, Adrenalinum, Dopamine Hydrochloride, Gaba (gamma Aminobutyric Acid), Norepinephrine, Octopamine, Serotonin (hydrochloride), Taurine, Adenosinum Cyclophosphoricum, Cerebrum (suis), Diencephalon (suis), Pineal Gland (suis), Thalamus Opticus (suis)

NDC Product Code 62185-0011

NDC 62185-0011-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Brain Support with NDC 62185-0011 is a a human over the counter drug product labeled by Dr. Donna Restivo Dc. The generic name of Brain Support is acetylcholine chloride, adrenalinum, dopamine hydrochloride, gaba (gamma aminobutyric acid), norepinephrine, octopamine, serotonin (hydrochloride), taurine, adenosinum cyclophosphoricum, cerebrum (suis), diencephalon (suis), pineal gland (suis), thalamus opticus (suis). The product's dosage form is liquid and is administered via oral form.

Labeler Name: Dr. Donna Restivo Dc

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.

Product Type: Human Otc Drug 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.

Brain Support Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ACETYLCHOLINE CHLORIDE 6 [hp_X]/mL
  • EPINEPHRINE 6 [hp_X]/mL
  • DOPAMINE HYDROCHLORIDE 6 [hp_X]/mL
  • .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]/mL
  • NOREPINEPHRINE 6 [hp_X]/mL
  • OCTOPAMINE 6 [hp_X]/mL
  • SEROTONIN HYDROCHLORIDE 6 [hp_X]/mL
  • TAURINE 6 [hp_X]/mL
  • ADENOSINE CYCLIC PHOSPHATE 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

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.
  • Oral - Administration to or by way of the mouth.

Product Labeler Information

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

Labeler Name: Dr. Donna Restivo Dc
Labeler Code: 62185
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 02-27-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 07-13-2021 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Brain Support Product Label Images

Brain Support Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Acetylcholine Chloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adrenalinum 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Dopamine Hydrochloride 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Gaba (Gamma Aminobutyric Acid) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Norepinephrine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Octopamine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Serotonin (Hydrochloride) 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Taurine 6X, 12X, 30X, 200X, 12C, 30C, 60C, 200C, Adenosinum Cyclophosphoricum 8X, Cerebrum (Suis) 8X, Diencephalon 8X, Pineal Gland (Suis) 8X, Thalamus Opticus (Suis) 8X

Homeopathic Indications:

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

Warnings:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.If pregnant or breast-feeding, ask a health professional before use.Tamper seal: Sealed for your protection. Do not use if seal is broken or missing.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

10 drops under the tongue, 3 to 6 times per day or as directed by a health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingrendients:

Demineralized water, 25% ethanol

Questions:

Distributed by Dr. Donna Restivo DC, Wellness Consultant822 South Lake Blvd. Mahopac, New York 10541www.mahopacmassage.com • (845) 628-6286

Package Label Display:

DR. DONNA RESTIVO DCWELLNESS CONSULTANTNDC 62185-0011-1HOMEOPATHICBrain SUPPORT1 FL OZ (30 ml)

* Please review the disclaimer below.