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  5. NDC Package Code: 43742-2195-1 Gum Therapy

NDC Package 43742-2195-1 Gum Therapy

Aconitum Napellus,Arnica Montana,Bismuthum Subnitricum,Borax,Calcarea Fluorica,Calendula - 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:
43742-2195-1
Package Description:
30 mL in 1 BOTTLE, DROPPER
Product Code:
43742-2195
Proprietary Name:
Gum Therapy
Non-Proprietary Name:
Aconitum Napellus, Arnica Montana, Bismuthum Subnitricum, Borax, Calcarea Fluorica, Calendula Officinalis, Cistus Canadensis, Hepar Sulphuris Calcareum, Kali Phosphoricum, Kreosotum, Mercurius Vivus, Myrrha, Natrum Muriaticum, Sepia
Substance Name:
Aconitum Napellus Whole; Arnica Montana Whole; Bismuth Subnitrate; Calcium Fluoride; Calcium Sulfide; Calendula Officinalis Flowering Top; Dibasic Potassium Phosphate; Helianthemum Canadense; Mercury; Myrrh; Sepia Officinalis Juice; Sodium Borate; Sodium Chloride; Wood Creosote
Usage Information:
1-10 drops under the tongue, 3 times a day or as directed by a health professional. Consult a physician for use in children under 12 years of age.
11-Digit NDC Billing Format:
43742219501
Product Type:
Human Otc Drug
Labeler Name:
Deseret Biologicals
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:
08-28-2024
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 43742-2195-1?

The NDC Packaged Code 43742-2195-1 is assigned to a package of 30 ml in 1 bottle, dropper of Gum Therapy, a human over the counter drug labeled by Deseret Biologicals. The product's dosage form is liquid and is administered via oral form.

Is NDC 43742-2195 included in the NDC Directory?

Yes, Gum Therapy with product code 43742-2195 is active and included in the NDC Directory. The product was first marketed by Deseret Biologicals on August 28, 2024 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 43742-2195-1?

The 11-digit format is 43742219501. 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
5-4-143742-2195-15-4-243742-2195-01