Ear Ring Liquid
NDC Package 43742-2001-1

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

Package Information

Ear Ring (allium cepa, argentum nitricum, chenopodium anthelminticum, dulcamara, ginkgo biloba, chininum sulphuricum, cartilago suis, mucosa nasalis suis, asarum canadense, onosmodium virginianum, natrum salicylicum, carbo vegetabilis, carboneum sulphuratum, cyclamen europaeum, gossypium herbaceum, graphites, kreosotum, phosphorus, plumbum metallicum, theridion, zincum metallicum) liquids is for the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .****These statements are based upon homeopathic principles. This formulation utilizes a liquid delivery system. Marketed by Deseret Biologicals, Inc., this product is identified by NDC 43742-2001.

Identification & Billing

NDC Package Code
43742-2001-1
Package Description
30 mL in 1 BOTTLE, DROPPER
Product Code
43742-2001
11-Digit Billing Format
43742200101

Clinical Specifications

Proprietary Name
Ear Ring
Non-Proprietary Name
Allium Cepa, Argentum Nitricum, Chenopodium Anthelminticum, Dulcamara, Ginkgo Biloba, Chininum Sulphuricum, Cartilago Suis, Mucosa Nasalis Suis, Asarum Canadense, Onosmodium Virginianum, Natrum Salicylicum, Carbo Vegetabilis, Carboneum Sulphuratum, Cyclamen Europaeum, Gossypium Herbaceum, Graphites, Kreosotum, Phosphorus, Plumbum Metallicum, Theridion, Zincum Metallicum
Substance Name
Onion; Silver Nitrate; Dysphania Ambrosioides Whole; Solanum Dulcamara Top; Ginkgo; Quinine Sulfate; Sus Scrofa Cartilage; Sus Scrofa Nasal Mucosa; Asarum Canadense Root; Onosmodium Virginianum; Sodium Salicylate; Activated Charcoal; Carbon Disulfide; Cyclamen Purpurascens Tuber; Gossypium Herbaceum Root Bark; Graphite; Wood Creosote; Phosphorus; Lead; Theridion Curassavicum; Zinc
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 the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .****These statements are based upon homeopathic principles. They have not been reviewed by the Food and Drug Administration. For the temporary relief of symptoms related to tinnitus, such as noises in ear following injury, decreased hearing, sensitivity to noise, noises with motion .****These statements are based upon homeopathic principles. 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
12-21-2020
End Marketing Date
12-01-2028
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 43742-2001-1 identifies a specific commercial package of 30 ml in 1 bottle, dropper of Ear Ring, a human over the counter drug labeled by Deseret Biologicals, Inc.. This liquid is formulated for oral use and contains onion; silver nitrate; dysphania ambrosioides whole; solanum dulcamara top; ginkgo; quinine sulfate; sus scrofa cartilage; sus scrofa nasal mucosa; asarum canadense root; onosmodium virginianum; sodium salicylate; activated charcoal; carbon disulfide; cyclamen purpurascens tuber; gossypium herbaceum root bark; graphite; wood creosote; phosphorus; lead; theridion curassavicum; zinc 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 December 21, 2020.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 43742200101. 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)
43742-2001-1
11-Digit CMS (5-4-2)
43742-2001-01

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