Genuine First Aid - Home First Aid
NDC Package 52124-1200-1

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.

Genuine First Aid - Home First Aid is uses   for the temporary relief of minor aches and pains associated with headache ; muscular aches ; minor arthritis pain ; toothache ; common cold ; menstrual cramps ; for the reduction of fever. Marketed by Genuine First Aid, Llc, this product is identified by NDC 52124-1200 and is authorized under FDA application part333E.

Identification & Billing

NDC Package Code
52124-1200-1
Package Description
1 KIT in 1 KIT * .5 mL in 1 PACKAGE (52124-0002-1) * .8 mL in 1 PACKAGE (52124-0001-1) * 2 TABLET, FILM COATED in 1 PACKET (47682-175-46) * 2 TABLET in 1 PACKET (52124-0009-1) * .5 g in 1 TUBE (52124-0003-1)
Product Code
52124-1200
11-Digit Billing Format
52124120001
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Genuine First Aid - Home First Aid
Dosage Form
-
Usage Information
Uses   for the temporary relief of minor aches and pains associated with headache ; muscular aches ; minor arthritis pain ; toothache ; common cold ; menstrual cramps ; for the reduction of fever

Regulatory & Marketing

Labeler Name
Genuine First Aid, Llc
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
01-11-2011
Listing Expiration
12-31-2017
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 52124-1200-1 identifies a specific commercial package of 1 kit in 1 kit * .5 ml in 1 package (52124-0002-1) * .8 ml in 1 package (52124-0001-1) * 2 tablet, film coated in 1 packet (47682-175-46) * 2 tablet in 1 packet (52124-0009-1) * .5 g in 1 tube (52124-0003-1) of Genuine First Aid - Home First Aid, labeled by Genuine First Aid, Llc. 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 Genuine First Aid, Llc on January 11, 2011. The current certification is valid through December 31, 2017.

How is this Genuine First Aid, Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52124120001. 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)
52124-1200-1
11-Digit CMS (5-4-2)
52124-1200-01

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