NDC Package 50181-0041-1 Neurobalance Pro

Adrenocorticotrophin,Gaba,Glutamic Acid,Norepinephrine,Acetylcholine - View Billable Units, 11-Digit Format, RxNorm

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
50181-0041-1
Package Description:
30 mL in 1 BOTTLE, SPRAY
Product Code:
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
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; Thyroid, Porcine
Usage Information:
For the temporary relief of loss of memory, metal weakness, senile dementia, forgetfulness, confusion, anxiety, brain fog, children with slow mental and physical development. For the temporary relief of loss of memory, metal weakness, senile dementia, forgetfulness, confusion, anxiety, brain fog, children with slow mental and physical development.
11-Digit NDC Billing Format:
50181004101
Product Type:
Human Otc Drug
Labeler Name:
The Wellness Center For Reseach And Education, Inc.
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):
  • Oral - Administration to or by way of the mouth.
  • Sample Package:
    No
    Marketing Category:
    UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
    Start Marketing Date:
    10-02-2015
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N

    The NDC Directory contains ONLY information on final marketed drugs submitted to FDA electronically by labelers. A labeler might be a manufacturer, re-packager or re-labeler. The product information included in the NDC directory does not indicate that FDA has verified the information provided by the product labeler. Assigned NDC numbers are not in any way an indication of FDA approval of the product.

    * Please review the disclaimer below.

    Frequently Asked Questions

    What is NDC 50181-0041-1?

    The NDC Packaged Code 50181-0041-1 is assigned to a package of 30 ml in 1 bottle, spray of Neurobalance Pro, a human over the counter drug labeled by The Wellness Center For Reseach And Education, Inc.. The product's dosage form is liquid and is administered via oral form.

    Is NDC 50181-0041 included in the NDC Directory?

    Yes, Neurobalance Pro with product code 50181-0041 is active and included in the NDC Directory. The product was first marketed by The Wellness Center For Reseach And Education, Inc. on October 02, 2015 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the 11-digit format for NDC 50181-0041-1?

    The 11-digit format is 50181004101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-4-1 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-4-150181-0041-15-4-250181-0041-01