Sting Relief
NDC Package 0924-5200-03

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

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

Sting Relief is packets are not child resistant. Marketed by Acme United Corporation, this product is identified by NDC 0924-5200 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
0924-5200-03
Package Description
50 PACKET in 1 BOX / .9 mL in 1 PACKET (0924-5200-01)
Product Code
0924-5200
11-Digit Billing Format
00924520003
RxNorm Crosswalk
  • RxCUI: 1190560 - ethanol 50 % / lidocaine HCl 2 % Medicated Pad
  • RxCUI: 1190560 - ethanol 0.5 ML/ML / lidocaine hydrochloride 20 MG/ML Medicated Pad
  • RxCUI: 1190560 - ethanol 50 % / lidocaine hydrochloride 2 % Medicated Pad

Clinical Specifications

Proprietary Name
Sting Relief
Dosage Form
-
Usage Information
Packets are not child resistant. Tamper evident packaging, do not use if packet is opened or torn.

Regulatory & Marketing

Labeler Name
Acme United Corporation
FDA Application #
part333E
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
03-06-2012
Listing Expiration
12-31-2020
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (0924-5200). Click a package code to view its specific billing and regulatory data.

0924-5200-02
10 PACKET in 1 BOX / .9 mL in 1 PACKET (0924-5200-01)

* 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 0924-5200-03 identifies a specific commercial package of 50 packet in 1 box / .9 ml in 1 packet (0924-5200-01) of Sting Relief, labeled by Acme United Corporation. 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 Acme United Corporation on March 06, 2012. The current certification is valid through December 31, 2020.

How is this Acme United Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 00924520003. 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 (4-4-2)
0924-5200-03
11-Digit CMS (5-4-2)
00924-5200-03

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