Genuine First Aid Burn Antiseptic Pain Relief With Aloe
NDC Package 52124-0004-2

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.

Genuine First Aid Burn Antiseptic Pain Relief With Aloe is wipe Injection site vigorously and discard. Marketed by Genuine First Aid, this product is identified by NDC 52124-0004 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
52124-0004-2
Package Description
6 PACKET in 1 BOX / .9 g in 1 PACKET
Product Code
52124-0004
11-Digit Billing Format
52124000402
RxNorm Crosswalk
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine HCl 0.5 % Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 1.3 MG/ML / lidocaine hydrochloride 5 MG/ML Topical Cream
  • RxCUI: 1012100 - benzalkonium chloride 0.13 % / lidocaine hydrochloride 0.5 % Topical Cream
  • RxCUI: 1046313 - benzocaine 6 % / ethanol 60 % Medicated Pad
  • RxCUI: 1046313 - benzocaine 60 MG/ML / ethanol 0.6 ML/ML Medicated Pad

Clinical Specifications

Proprietary Name
Genuine First Aid Burn Antiseptic Pain Relief With Aloe
Dosage Form
-
Usage Information
Wipe Injection site vigorously and discard. Adults and children 2 years of age and olderclean affected area.apply a small amount of this product on the area 1 to 3 times daily.may be covered with a sterile bandagechildren under 2 years of age: consult a doctor Clean intended area thoroughly with pad. Discard after single use.

Regulatory & Marketing

Labeler Name
Genuine First Aid
FDA Application #
part333A
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-23-2010
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (52124-0004). Click a package code to view its specific billing and regulatory data.

52124-0004-1
.9 g in 1 PACKET
52124-0004-3
100 PACKET in 1 CARTON / .9 g in 1 PACKET

* 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 52124-0004-2 identifies a specific commercial package of 6 packet in 1 box / .9 g in 1 packet of Genuine First Aid Burn Antiseptic Pain Relief With Aloe, labeled by Genuine First Aid. 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 on April 23, 2010. The current certification is valid through December 31, 2017.

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

For medical billing and reimbursement, this package follows the 11-digit CMS format: 52124000402. 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)
52124-0004-2
11-Digit CMS (5-4-2)
52124-0004-02

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