Dentaforce Liquid
NDC Package 43857-0093-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Dentaforce (antimonium crudum, belladonna, calcarea carbonica, calcarea fluorica, calcarea phosphorica, hekla lava, mercurius solubilis, plumbum metallicum, sepia, silicea, hydrofluoricum acidum) liquids is for temporary relief of gum, dentition, and tooth pain. This formulation utilizes a liquid delivery system. Marketed by Bioactive Nutritional, Inc., this product is identified by NDC 43857-0093.

Identification & Billing

NDC Package Code
43857-0093-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43857-0093
11-Digit Billing Format
43857009301

Clinical Specifications

Proprietary Name
Dentaforce
Non-Proprietary Name
Antimonium Crudum, Belladonna, Calcarea Carbonica, Calcarea Fluorica, Calcarea Phosphorica, Hekla Lava, Mercurius Solubilis, Plumbum Metallicum, Sepia, Silicea, Hydrofluoricum Acidum
Substance Name
Antimony Trisulfide; Atropa Belladonna; Calcium Fluoride; Hekla Lava; Hydrofluoric Acid; Lead; Mercurius Solubilis; Oyster Shell Calcium Carbonate, Crude; Sepia Officinalis Juice; Silicon Dioxide; Tribasic Calcium Phosphate
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
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Pharmacologic Class
Usage Information
For temporary relief of gum, dentition, and tooth pain. For temporary relief of gum, dentition, and tooth pain.

Regulatory & Marketing

Labeler Name
Bioactive Nutritional, Inc.
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
09-10-2013
Listing Expiration
12-31-2027
Exclude Flag
N
Sample Package
No

Hierarchy Structure

Code Lineage

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 full disclaimer at the bottom of this page.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 43857-0093-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Dentaforce, a human over the counter drug labeled by Bioactive Nutritional, Inc.. This liquid is formulated for oral use and contains antimony trisulfide; atropa belladonna; calcium fluoride; hekla lava; hydrofluoric acid; lead; mercurius solubilis; oyster shell calcium carbonate, crude; sepia officinalis juice; silicon dioxide; tribasic calcium phosphate as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Bioactive Nutritional, Inc. on September 10, 2013. The current certification is valid through December 31, 2027.

How is this Bioactive Nutritional, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43857009301. The table below illustrates the segment conversion from the 10-digit labeler code to the 11-digit provider format.

11-Digit Code Conversion

Billing payers usually require a 5-4-2 segment configuration. Below is the conversion from the 10-digit package format to the 11-digit billing format:

10-Digit Format (5-4-1)
43857-0093-1
11-Digit CMS (5-4-2)
43857-0093-01

Note: The zero is added to the Package segment to maintain the 5-4-2 structure.