50181-0041 NDC - NEUROBALANCE PRO (ADRENOCORTICOTROPHIN, GABA, GLUTAMIC ACID, NOREPINEPHRINE, ACETYLCHOLINE CHLORIDE, ADRENALINUM, L-DOPA, SEROTONIN (HYDROCHLORIDE), THYROIDINUM (SUIS), ANACARDIUM ORIENTALE, BARYTA CARBONICA, CALCAREA CARBONICA, STRAMONIUM)

Drug Information

  • Product NDC: 50181-0041
  • Proprietary Name: Neurobalance Pro
  • Non Proprietary Name: Adrenocorticotrophin, GABA, Glutamic Acid, Norepinephrine, Acetylcholine Chloride, Adrenalinum, L-Dopa, Serotonin (Hydrochloride), Thyroidinum (Suis), Anacardium Orientale, Baryta Carbonica, Calcarea Carbonica, Stramonium
  • Active Ingredient(s): 6 [hp_X]/mL .GAMMA.-AMINOBUTYRIC ACID; 6 [hp_X]/mL ACETYLCHOLINE CHLORIDE; 6 [hp_C]/mL BARIUM CARBONATE; 6 [hp_X]/mL CORTICOTROPIN; 30 [hp_C]/mL DATURA STRAMONIUM; 6 [hp_X]/mL EPINEPHRINE; 6 [hp_X]/mL GLUTAMIC ACID; 6 [hp_X]/mL LEVODOPA; 6 [hp_X]/mL NOREPINEPHRINE; 6 [hp_C]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 6 [hp_C]/mL SEMECARPUS ANACARDIUM JUICE; 6 [hp_X]/mL SEROTONIN HYDROCHLORIDE; 6 [hp_X]/mL THYROID
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Adrenergic alpha-Agonists [MoA]; Adrenergic beta-Agonists [MoA]; Adrenocorticotropic Hormone [CS]; Adrenocorticotropic Hormone [EPC]; Amino Acids; Aromatic [CS]; Aromatic Amino Acid [EPC]; Catecholamine [EPC]; Catecholamine [EPC]; Catecholamines [CS]; Catecholamines [CS]; Cholinergic Agonists [MoA]; Cholinergic Receptor Agonist [EPC]; alpha-Adrenergic Agonist [EPC]; beta-Adrenergic Agonist [EPC]

Labeler Information

Field Name Field Value
Labeler Name: The Wellness Center for Reseach and Education, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:10/2/2015
End Marketing Date:8/1/2025

Package Information

No. Package Code Package Description Billing Unit
150181-0041-130 mL in 1 BOTTLE, SPRAY (50181-0041-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC50181-0041The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMENeurobalance ProThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAdrenocorticotrophin, GABA, Glutamic Acid, Norepinephrine, Acetylcholine Chloride, Adrenalinum, L-Dopa, Serotonin (Hydrochloride), Thyroidinum (Suis), Anacardium Orientale, Baryta Carbonica, Calcarea Carbonica, StramoniumThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE10/2/2015This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE8/1/2025This 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.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEThe Wellness Center for Reseach and Education, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME.GAMMA.-AMINOBUTYRIC ACID; ACETYLCHOLINE CHLORIDE; BARIUM CARBONATE; CORTICOTROPIN; DATURA STRAMONIUM; EPINEPHRINE; GLUTAMIC ACID; LEVODOPA; NOREPINEPHRINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SEMECARPUS ANACARDIUM JUICE; SEROTONIN HYDROCHLORIDE; THYROIDAn 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.
ACTIVE NUMERATOR STRENGTH6; 6; 6; 6; 30; 6; 6; 6; 6; 6; 6; 6; 6 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/mL; [hp_C]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAdrenergic alpha-Agonists [MoA], Adrenergic beta-Agonists [MoA], Adrenocorticotropic Hormone [CS], Adrenocorticotropic Hormone [EPC], Amino Acids, Aromatic [CS], Aromatic Amino Acid [EPC], Catecholamine [EPC], Catecholamine [EPC], Catecholamines [CS], Catecholamines [CS], Cholinergic Agonists [MoA], Cholinergic Receptor Agonist [EPC], alpha-Adrenergic Agonist [EPC], beta-Adrenergic Agonist [EPC] 

Download Record

Download this NDC record record in Text format: Export

Download this NDC record record in Excel (CSV) format: Export

Download this NDC record record in XML format: Export

This page was last updated on: 7/4/2025

Previous Code
Next Code