50 Person Ansi
NDC Package 52124-0113-1

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.

50 Person Ansi is a medication used as Purpose: First aid antiseptic, external analgesicUses: First aid to help prevent infection and for the temporary relief of pain and itching associated with: Minor CutsScrapesBurns Use: For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water. Marketed by Genuine First Aid Llc, this product is identified by NDC 52124-0113 and is authorized under FDA application part333.

Identification & Billing

NDC Package Code
52124-0113-1
Package Description
1 KIT in 1 KIT * .9 g in 1 PACKAGE (52124-0006-1) * .5 mL in 1 PACKAGE (52124-0002-1) * 2 TABLET in 1 PACKAGE (52124-0011-1) * 2 TABLET in 1 PACKAGE (52124-0010-1) * 2 TABLET in 1 PACKAGE (52124-0009-1) * .5 mL in 1 PACKAGE (52124-0008-1) * 10 mL in 1 BOTTLE (52124-0005-1) * .5 g in 1 TUBE (52124-0003-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .9 g in 1 PACKAGE (52124-0004-1)
Product Code
52124-0113
11-Digit Billing Format
52124011301
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: 1038561 - benzalkonium Cl 0.4 % Medicated Pad
  • RxCUI: 1038561 - benzalkonium chloride 4 MG/ML Medicated Pad

Clinical Specifications

Proprietary Name
50 Person Ansi
Dosage Form
-
Usage Information
This product is used as Purpose: First aid antiseptic, external analgesicUses: First aid to help prevent infection and for the temporary relief of pain and itching associated with: Minor CutsScrapesBurns Use: For Professional and Hospital use.  Helps prevent infection.  Antiseptic cleansing of face, hands and body without soap and water. Uses:  To help prevent infection in: minor cuts;  scrapes;  burns Uses:For flushing or irrigating the eyes toremove loose foreign material, air pollutants, or chlorinated water. Use: For the temporary relief of pain and itching associated with minor burns, scrapes and insect bites. Uses temporarily relieves minor aches and pains due to:the common coldheadachetoothachemuscular achesbackacheminor pain of arthritismenstrual cramps temporarily reduces fever Usestemporary relief of minor aches and pains associated with:common cold;  headache; toothache; muscular aches;  backache; arthritis; menstrual cramps;  and reduction of fever Uses    Temporarily relieves minor aches and pains associated with:headache ; muscular aches ; minor arthritis pain ; backache ; common cold ; toothache ; menstrual cramps ; Temporarily reduces fever Use:    For preparation of skin before injection. Enter section text here

Regulatory & Marketing

Labeler Name
Genuine First Aid Llc
FDA Application #
part333
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-02-2010
Listing Expiration
12-31-2018
Exclude Flag
I
Sample Package
No

Hierarchy Structure

Code Lineage
  • 52124 - Genuine First Aid Llc
    • 52124-0113 - 50 Person Ansi
      • 52124-0113-1 - 1 KIT in 1 KIT * .9 g in 1 PACKAGE (52124-0006-1) * .5 mL in 1 PACKAGE (52124-0002-1) * 2 TABLET in 1 PACKAGE (52124-0011-1) * 2 TABLET in 1 PACKAGE (52124-0010-1) * 2 TABLET in 1 PACKAGE (52124-0009-1) * .5 mL in 1 PACKAGE (52124-0008-1) * 10 mL in 1 BOTTLE (52124-0005-1) * .5 g in 1 TUBE (52124-0003-1) * .8 mL in 1 PACKAGE (52124-0001-1) * .9 g in 1 PACKAGE (52124-0004-1)

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 52124-0113-1 identifies a specific commercial package of 1 kit in 1 kit * .9 g in 1 package (52124-0006-1) * .5 ml in 1 package (52124-0002-1) * 2 tablet in 1 package (52124-0011-1) * 2 tablet in 1 package (52124-0010-1) * 2 tablet in 1 package (52124-0009-1) * .5 ml in 1 package (52124-0008-1) * 10 ml in 1 bottle (52124-0005-1) * .5 g in 1 tube (52124-0003-1) * .8 ml in 1 package (52124-0001-1) * .9 g in 1 package (52124-0004-1) of 50 Person Ansi, 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 June 02, 2010. The current certification is valid through December 31, 2018.

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: 52124011301. 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)
52124-0113-1
11-Digit CMS (5-4-2)
52124-0113-01

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