Tidl Pain Relief Numbing Patch
NDC Package 83822-003-01

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

Package Information

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

Tidl Pain Relief Numbing Patch is adults and children 12 years of age and older: -clean and dry affected area -remove backing from patch by firmly grasping both ends and gently pulling until backing seprarates in middle -carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area -once exposed portion of the patch is positioned,carefully remove remaining backing to completely apply patch to affected area - use 1 patch at a time and not more than 3 to 4 times daily Children under 12 years of age: consult a doctor. Marketed by Fuzhou Ayimong Trading Co., Ltd., this product is identified by NDC 83822-003 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
83822-003-01
Package Description
20 PATCH in 1 BOX
Product Code
83822-003
11-Digit Billing Format
83822000301
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Tidl Pain Relief Numbing Patch
Dosage Form
-
Usage Information
Adults and children 12 years of age and older: -clean and dry affected area -remove backing from patch by firmly grasping both ends and gently pulling until backing seprarates in middle -carefully remove smaller portion of backing from patch and apply exposed portion of patch to affected area -once exposed portion of the patch is positioned,carefully remove remaining backing to completely apply patch to affected area - use 1 patch at a time and not more than 3 to 4 times daily Children under 12 years of age: consult a doctor

Regulatory & Marketing

Labeler Name
Fuzhou Ayimong Trading Co., Ltd.
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
03-24-2024
Listing Expiration
12-31-2025
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 83822-003-01 identifies a specific commercial package of 20 patch in 1 box of Tidl Pain Relief Numbing Patch, labeled by Fuzhou Ayimong Trading Co., Ltd.. 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 Fuzhou Ayimong Trading Co., Ltd. on March 24, 2024. The current certification is valid through December 31, 2025.

How is this Fuzhou Ayimong Trading Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 83822000301. 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)
83822-003-01
11-Digit CMS (5-4-2)
83822-0003-01

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