First Aid Antiseptic Pain Relieving
NDC Package 50814-009-01

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 discontinued by the firm.

First Aid Antiseptic Pain Relieving is • Clean the affected area. Marketed by Gfa Production (xiamen) Co., Ltd., this product is identified by NDC 50814-009 and is authorized under FDA application M003.

Identification & Billing

NDC Package Code
50814-009-01
Package Description
.9 g in 1 PACKAGE
Product Code
50814-009
11-Digit Billing Format
50814000901
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: 1038558 - benzalkonium chloride 0.13 % Medicated Pad
  • RxCUI: 1038558 - benzalkonium chloride 1.3 MG/ML Medicated Pad

Clinical Specifications

Proprietary Name
First Aid Antiseptic Pain Relieving
Dosage Form
-
Usage Information
• Clean the affected area. • Apply a small amount of this product (an amount equal to the surface area of the tip of a finger) on the area 1 to 3 times daily. • May be covered with a sterile bandage. Clean the affected areaAdults and children 2 years of age and older: Apply a small amount of this product to affected area not more than 3 times dailyChildren under 2 years of age: consult a doctorMay be covered with a sterile bandage

Regulatory & Marketing

Labeler Name
Gfa Production (xiamen) Co., Ltd.
FDA Application #
M003
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-01-2016
End Marketing Date
09-01-2025
Listing Expiration
09-01-2025
Exclude Flag
D
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 50814-009-01 identifies a specific commercial package of .9 g in 1 package of First Aid Antiseptic Pain Relieving, labeled by Gfa Production (xiamen) Co., 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 Gfa Production (xiamen) Co., Ltd. on July 01, 2016. The current certification is valid through September 01, 2025.

How is this Gfa Production (xiamen) Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 50814000901. 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)
50814-009-01
11-Digit CMS (5-4-2)
50814-0009-01

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