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  5. NDC Package Code: 50181-0084-1 Mbm 13 Female

NDC Package 50181-0084-1 Mbm 13 Female

Phytolacca Decandra,Hypophysis (suis),Scrophularia Nodosa,Hypothalamus (suis),Calcarea - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

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:
50181-0084-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
50181-0084
Proprietary Name:
Mbm 13 Female
Non-Proprietary Name:
Phytolacca Decandra, Hypophysis (suis), Scrophularia Nodosa, Hypothalamus (suis), Calcarea Carbonica, Cimicifuga Racemosa, Lilium Tigrinum, Sulphur, Causticum, Graphites, Kali Phosphoricum
Substance Name:
Black Cohosh; Bos Taurus Hypothalamus; Causticum; Dibasic Potassium Phosphate; Graphite; Lilium Lancifolium Whole Flowering; Oyster Shell Calcium Carbonate, Crude; Phytolacca Americana Root; Scrophularia Nodosa Whole; Sulfur; Sus Scrofa Pituitary Gland
Usage Information:
For the temporary relief of emotionlessness, denial, numbness, and unresponsiveness. For the temporary relief of emotionlessness, denial, numbness, and unresponsiveness.
11-Digit NDC Billing Format:
50181008401
Product Type:
Human Otc Drug
Labeler Name:
The Wellness Center For Research 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.
Active Ingredient(s):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
05-03-2022
End Marketing Date:
06-09-2027
Exclude Flag:
N
Code Structure:

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 50181-0084-1?

The NDC Packaged Code 50181-0084-1 is assigned to a package of 30 ml in 1 bottle, dropper of Mbm 13 Female, a human over the counter drug labeled by The Wellness Center For Research And Education, Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 50181-0084 included in the NDC Directory?

Yes, Mbm 13 Female with product code 50181-0084 is active and included in the NDC Directory. The product was first marketed by The Wellness Center For Research And Education, Inc. on May 03, 2022.

What is the 11-digit format for NDC 50181-0084-1?

The 11-digit format is 50181008401. 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
5-4-150181-0084-15-4-250181-0084-01