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  5. NDC Package Code: 43857-0593-1 Dentox

NDC Package 43857-0593-1 Dentox

Berberis Vulgaris,Glycyrrhiza Glabra,Lappa Major,Stillingia Sylvatica,Trifolium - 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:
43857-0593-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43857-0593
Proprietary Name:
Dentox
Non-Proprietary Name:
Berberis Vulgaris, Glycyrrhiza Glabra, Lappa Major, Stillingia Sylvatica, Trifolium Pratense, Phytolacca Decandra, Lymph Node(suis), Medulla Ossis Suis, Thymus (suis), Thyroidinum (suis), Calcarea Fluorica, Natrum Fluoratum, Argentum Metallicum, Aurum Metallicum, Cuprum Metallicum, Eugenol, Formalinum, Lidocaine, Mercurius Solubilis, Molybdenum, Niccolum Metallicum, Palladium Metallicum, Stannum Metallicum, Titanium Metallicum, Zincum Metallicum
Substance Name:
Arctium Lappa Root; Berberis Vulgaris Root Bark; Calcium Fluoride; Copper; Eugenol; Formaldehyde Solution; Glycyrrhiza Glabra; Gold; Lidocaine; Mercurius Solubilis; Molybdenum; Nickel; Palladium; Phytolacca Americana Root; Silver; Sodium Fluoride; Stillingia Sylvatica Root; Sus Scrofa Bone Marrow; Sus Scrofa Lymph; Sus Scrofa Thymus; Thyroid; Tin; Titanium; Trifolium Pratense Flower; Zinc
Usage Information:
10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
43857059301
Product Type:
Human Otc Drug
Labeler Name:
Bioactive Nutritional, 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):
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:
02-14-2023
Listing Expiration Date:
12-31-2025
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 43857-0593-1?

The NDC Packaged Code 43857-0593-1 is assigned to a package of 30 ml in 1 bottle, dropper of Dentox, a human over the counter drug labeled by Bioactive Nutritional, Inc.. The product's dosage form is liquid and is administered via oral form.

Is NDC 43857-0593 included in the NDC Directory?

Yes, Dentox with product code 43857-0593 is active and included in the NDC Directory. The product was first marketed by Bioactive Nutritional, Inc. on February 14, 2023 and its listing in the NDC Directory is set to expire on December 31, 2025 if the product is not updated or renewed by the manufacturer.

What is the 11-digit format for NDC 43857-0593-1?

The 11-digit format is 43857059301. 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
5-4-143857-0593-15-4-243857-0593-01