Screamin Hot Toast
NDC Package 52099-8005-1

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.

Screamin Hot Toast is directions apply to the region of specific pain or injury, reapply up to three times per daily, wash hands thoroughly in the event of contact, because activation takes about 1 hour, first time users should apply a small amount and increase gradually on reapplications depending on reaction.For use on children under the age of 12 consult a physician. Marketed by Q.a. Laboratories, this product is identified by NDC 52099-8005 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
52099-8005-1
Package Description
141 g in 1 TUBE
Product Code
52099-8005
11-Digit Billing Format
52099800501
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Screamin Hot Toast
Dosage Form
-
Usage Information
Directions apply to the region of specific pain or injury, reapply up to three times per daily, wash hands thoroughly in the event of contact, because activation takes about 1 hour, first time users should apply a small amount and increase gradually on reapplications depending on reaction.For use on children under the age of 12 consult a physician. Arthritis sufferers: Apply three times daily for two weeks. Wait twenty minutes before washing arthritic hands. Thereafter use as needed.

Regulatory & Marketing

Labeler Name
Q.a. Laboratories
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
06-19-2012
Listing Expiration
12-31-2023
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 52099-8005-1 identifies a specific commercial package of 141 g in 1 tube of Screamin Hot Toast, labeled by Q.a. Laboratories. 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 Q.a. Laboratories on June 19, 2012. The current certification is valid through December 31, 2023.

How is this Q.a. Laboratories product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52099800501. 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)
52099-8005-1
11-Digit CMS (5-4-2)
52099-8005-01

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