Sting-kill
NDC Package 52412-250-20

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-kill is children under 2 yrs.▪Do not use▪Consult doctorAdults and children 2 yrs. Marketed by Randob Ltd., this product is identified by NDC 52412-250 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
52412-250-20
Package Description
8 POUCH in 1 BLISTER PACK / .56 mL in 1 POUCH
Product Code
52412-250
11-Digit Billing Format
52412025020
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sting-kill
Dosage Form
-
Usage Information
Children under 2 yrs.▪Do not use▪Consult doctorAdults and children 2 yrs. and older▪Apply to affected area as needed but not more than 3 to 4 times a day.▪(1) Bee stings only, remove stinger before treatment.▪(2) Tear foil pack at notch, exposing pad.▪(3) Apply immediately to bite or sting area. Dispose of pad after use.

Regulatory & Marketing

Labeler Name
Randob Ltd.
FDA Application #
part348
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
01-01-1965
Listing Expiration
12-31-2022
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 (52412-250). Click a package code to view its specific billing and regulatory data.

52412-250-21
8 POUCH in 1 CARTON / .56 mL in 1 POUCH

* 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 52412-250-20 identifies a specific commercial package of 8 pouch in 1 blister pack / .56 ml in 1 pouch of Sting-kill, labeled by Randob 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 Randob Ltd. on January 01, 1965. The current certification is valid through December 31, 2022.

How is this Randob Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52412025020. 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)
52412-250-20
11-Digit CMS (5-4-2)
52412-0250-20

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