Sting Relief Medicated Pad
NDC Package 71222-002-01

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.

Sting Relief Medicated Pad is apply to affected area not more than 3 to 4 times daily. Marketed by Tongzhou Deqi Medical Products Factory, this product is identified by NDC 71222-002 and is authorized under FDA application part333B.

Identification & Billing

NDC Package Code
71222-002-01
Package Description
1 SWAB in 1 PACKET
Product Code
71222-002
11-Digit Billing Format
71222000201
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sting Relief Medicated Pad
Dosage Form
-
Usage Information
Apply to affected area not more than 3 to 4 times daily. For adults and children 2 years of age and older. Children under 2 years: consult a physician. 

Regulatory & Marketing

Labeler Name
Tongzhou Deqi Medical Products Factory
FDA Application #
part333B
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
05-20-2013
Listing Expiration
12-31-2018
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 71222-002-01 identifies a specific commercial package of 1 swab in 1 packet of Sting Relief Medicated Pad, labeled by Tongzhou Deqi Medical Products Factory. 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 Tongzhou Deqi Medical Products Factory on May 20, 2013. The current certification is valid through December 31, 2018.

How is this Tongzhou Deqi Medical Products Factory product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 71222000201. 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)
71222-002-01
11-Digit CMS (5-4-2)
71222-0002-01

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