T Relief Arthritis Extra Strength
NDC Package 62795-1053-2

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

T Relief Arthritis Extra Strength is for max absorption, dissolve under tongue.Can be chewed and swallowed. Marketed by Medinatura Inc, this product is identified by NDC 62795-1053.

Identification & Billing

NDC Package Code
62795-1053-2
Package Description
250 TABLET in 1 BOTTLE
Product Code
11-Digit Billing Format
62795105302
Billing Unit
EA - Billing unit of "each" is used when the product is dispensed in discreet units.
Units Per Package
250 EA

Clinical Specifications

Proprietary Name
T Relief Arthritis Extra Strength
Dosage Form
-
Usage Information
For max absorption, dissolve under tongue.Can be chewed and swallowed. Adults: 2 tablets every4 hours. Do not exceed 12 tablets per 24 hours.Children under 18 years: consult your health professional

Regulatory & Marketing

Labeler Name
Medinatura Inc
Marketing Category
UNAPPROVED HOMEOPATHIC - A category specifying that a product is marketed as unapproved homeopathic product.
Start Marketing Date
04-05-2022
Listing Expiration
12-31-2024
Exclude Flag
I
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 62795-1053-2 identifies a specific commercial package of 250 tablet in 1 bottle of T Relief Arthritis Extra Strength, labeled by Medinatura Inc. This product is billed for "EA" each discreet unit and contains an estimated amount of 250 billable units per package. This is formulated for use and contains as the active substance.

Is this product currently listed with the FDA?

This product code is currently listed as inactive or excluded from the primary directory. It was introduced to the market by Medinatura Inc on April 05, 2022. The current certification is valid through December 31, 2024.

How is this Medinatura Inc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 62795105302. Quantities are measured in per "each", products billed on a per each basis are usually products dispensed in discreet units.. There are 250 total billable units per package. 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)
62795-1053-2
11-Digit CMS (5-4-2)
62795-1053-02

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