Celeragesic Gel
NDC Package 43742-1397-1

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

Package Information

Celeragesic (echinacea (angustifolia), calendula officinalis, hamamelis virginiana, echinacea purpurea, bellis perennis, chamomilla, hypericum perforatum, millefolium, ledum palustre, arnica montana, bryonia (alba), hepar sulphuris calcareum, nadidum, pantothenic acid, sarcolacticum acidum, symphytum officinale, rhus tox, aconitum napellus, funiculus umbilicalis suis, glandula suprarenalis suis) gel is for the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. This formulation utilizes a gel delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-1397.

Identification & Billing

NDC Package Code
43742-1397-1
Package Description
57 g in 1 TUBE
Product Code
43742-1397
11-Digit Billing Format
43742139701

Clinical Specifications

Proprietary Name
Celeragesic
Non-Proprietary Name
Echinacea (angustifolia), Calendula Officinalis, Hamamelis Virginiana, Echinacea Purpurea, Bellis Perennis, Chamomilla, Hypericum Perforatum, Millefolium, Ledum Palustre, Arnica Montana, Bryonia (alba), Hepar Sulphuris Calcareum, Nadidum, Pantothenic Acid, Sarcolacticum Acidum, Symphytum Officinale, Rhus Tox, Aconitum Napellus, Funiculus Umbilicalis Suis, Glandula Suprarenalis Suis
Substance Name
Achillea Millefolium Whole; Aconitum Napellus Whole; Arnica Montana Whole; Bellis Perennis Whole; Bryonia Alba Root; Calcium Sulfide; Calendula Officinalis Flowering Top; Comfrey Root; Echinacea Angustifolia Whole; Echinacea Purpurea Whole; Hamamelis Virginiana Root Bark/stem Bark; Hypericum Perforatum Whole; Lactic Acid, L-; Matricaria Chamomilla Whole; Nadide; Pantothenic Acid; Rhododendron Tomentosum Leafy Twig; Sus Scrofa Adrenal Gland; Sus Scrofa Umbilical Cord; Toxicodendron Pubescens Leaf
Dosage Form
Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
Usage Information
For the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration. For the temporary relief of muscular pain, joint pain, sports injuries and bruising.****These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Deseret Biologicals, 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
10-31-2018
End Marketing Date
03-04-2029
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 43742-1397-1 identifies a specific commercial package of 57 g in 1 tube of Celeragesic, a human over the counter drug labeled by Deseret Biologicals, Inc.. This gel is formulated for topical use and contains achillea millefolium whole; aconitum napellus whole; arnica montana whole; bellis perennis whole; bryonia alba root; calcium sulfide; calendula officinalis flowering top; comfrey root; echinacea angustifolia whole; echinacea purpurea whole; hamamelis virginiana root bark/stem bark; hypericum perforatum whole; lactic acid, l-; matricaria chamomilla whole; nadide; pantothenic acid; rhododendron tomentosum leafy twig; sus scrofa adrenal gland; sus scrofa umbilical cord; toxicodendron pubescens leaf 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 Deseret Biologicals, Inc. on October 31, 2018.

How is this Deseret Biologicals, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742139701. 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)
43742-1397-1
11-Digit CMS (5-4-2)
43742-1397-01

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