Ring Relief Liquid
NDC Package 17312-001-15

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

Package Information

Ring Relief (arnica montana, calcium sulfide, hypericum perforatum, lycopodium clavatum spore, thiosinaminum, mercurius solubilis, salicylic acid, silicon dioxide, allylthiourea) liquids is uses:* According to homeopathic indications, these ingredients temporarily relieve Tinnitus symptoms such as: • Ringing • Buzzing • Roaring • Nerve and Noise Sensitivity • Pounding • Discomfort • Wax buildup after serious causes have been ruled out by a physician. This formulation utilizes a liquid delivery system. Marketed by Trp Company, this product is identified by NDC 17312-001.

Identification & Billing

NDC Package Code
17312-001-15
Package Description
1 BOTTLE, DROPPER in 1 PACKAGE / 10 mL in 1 BOTTLE, DROPPER
Product Code
17312-001
11-Digit Billing Format
17312000115

Clinical Specifications

Proprietary Name
Ring Relief
Non-Proprietary Name
Arnica Montana, Calcium Sulfide, Hypericum Perforatum, Lycopodium Clavatum Spore, Thiosinaminum, Mercurius Solubilis, Salicylic Acid, Silicon Dioxide, Allylthiourea
Substance Name
Allylthiourea; Arnica Montana; Calcium Sulfide; Hypericum Perforatum; Lycopodium Clavatum Spore; Mercurius Solubilis; Salicylic Acid; Silicon Dioxide
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
Auricular (otic) - Administration to or by way of the ear.
Active Ingredient(s)
Usage Information
Uses:* According to homeopathic indications, these ingredients temporarily relieve Tinnitus symptoms such as: • Ringing • Buzzing • Roaring • Nerve and Noise Sensitivity • Pounding • Discomfort • Wax buildup after serious causes have been ruled out by a physician. *These statements are based upon traditional homeopathic practice. They have not been reviewed by the Food and Drug Administration.

Regulatory & Marketing

Labeler Name
Trp Company
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
06-01-2006
Listing Expiration
12-31-2026
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (17312-001). Click a package code to view its specific billing and regulatory data.

17312-001-11
1 BOTTLE, DROPPER in 1 PACKAGE / 15 mL in 1 BOTTLE, DROPPER

* 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 17312-001-15 identifies a specific commercial package of 1 bottle, dropper in 1 package / 10 ml in 1 bottle, dropper of Ring Relief, a human over the counter drug labeled by Trp Company. This liquid is formulated for auricular (otic) use and contains allylthiourea; arnica montana; calcium sulfide; hypericum perforatum; lycopodium clavatum spore; mercurius solubilis; salicylic acid; silicon dioxide 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 Trp Company on June 01, 2006. The current certification is valid through December 31, 2026.

How is this Trp Company product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 17312000115. 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 (5-3-2)
17312-001-15
11-Digit CMS (5-4-2)
17312-0001-15

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