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  5. NDC Package Code: 50181-0014-1 Biotox Para

NDC Package 50181-0014-1 Biotox Para

Cochlearia Armoracia,Toxoplasma Gondii,Vibrio Cholerae,Candida Albicans,Trichinella - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

This product is approaching its end of marketing date. An upcoming end of marketing date means the product has been delisted but will remain in the NDC database until the end of marketing date is reached. In most cases, the FDA advises firms to use the expiration date of the last lot produced as the end marketing date, reflecting the possibility that the product may still be available even after manufacturing has stopped.

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:
50181-0014-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
50181-0014
Proprietary Name:
Biotox Para
Non-Proprietary Name:
Cochlearia Armoracia, Toxoplasma Gondii, Vibrio Cholerae, Candida Albicans, Trichinella Spiralis
Substance Name:
Candida Albicans; Horseradish; Plasmodium Malariae; Taraxacum Officinale; Toxoplasma Gondii; Trichinella Spiralis; Trichophyton Rubrum; Vibrio Cholerae
Usage Information:
Allergies, distention of abdomen, edema, constipation, diarrhea, intestinal dysbiosis, flu-like symptoms, skin rash, ulcers, boils, fever, vomiting, immune system, intestinal hemorrhaging. 
11-Digit NDC Billing Format:
50181001401
Product Type:
Human Otc Drug
Labeler Name:
The Wellness Center
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):
Pharmacologic Class(es):
Sample Package:
No
Marketing Category:
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date:
06-07-2013
End Marketing Date:
10-07-2025
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 50181-0014-1?

The NDC Packaged Code 50181-0014-1 is assigned to a package of 30 ml in 1 bottle, dropper of Biotox Para, a human over the counter drug labeled by The Wellness Center. The product's dosage form is liquid and is administered via oral form.

Is NDC 50181-0014 included in the NDC Directory?

Yes, Biotox Para with product code 50181-0014 is active and included in the NDC Directory. The product was first marketed by The Wellness Center on June 07, 2013.

What is the 11-digit format for NDC 50181-0014-1?

The 11-digit format is 50181001401. 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
5-4-150181-0014-15-4-250181-0014-01