First Aid Triple Antibiotic And Pain Relief
NDC Package 51852-100-01

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 inactivated by the FDA.

First Aid Triple Antibiotic And Pain Relief is usesFirst aid to help prevent infection in minor cuts, scrapes, and burnsFirst aid for the temporary relief of pain in minor cuts, scrapes, and burns. Marketed by Lifelabs, A Division Of Atico International Usa, Inc., this product is identified by NDC 51852-100 and is authorized under FDA application part333B.

Identification & Billing

NDC Package Code
51852-100-01
Package Description
1 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code
51852-100
11-Digit Billing Format
51852010001
RxNorm Crosswalk
  • RxCUI: 1359350 - bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG in GM Topical Ointment
  • RxCUI: 1359350 - bacitracin 0.5 UNT/MG / neomycin 0.0035 MG/MG / polymyxin B 10 UNT/MG / pramoxine hydrochloride 0.01 MG/MG Topical Ointment
  • RxCUI: 1359350 - bacitracin 500 UNT / neomycin 3.5 MG / polymyxin B 10,000 UNT / pramoxine HCl 10 MG per GM Topical Ointment

Clinical Specifications

Proprietary Name
First Aid Triple Antibiotic And Pain Relief Maximum Strength
Dosage Form
-
Usage Information
UsesFirst aid to help prevent infection in minor cuts, scrapes, and burnsFirst aid for the temporary relief of pain in minor cuts, scrapes, and burns

Regulatory & Marketing

Labeler Name
Lifelabs, A Division Of Atico International Usa, Inc.
FDA Application #
part333B
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-01-2010
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.

Frequently Asked Questions

What is the distribution configuration for this product package?

The code 51852-100-01 identifies a specific commercial package of 1 tube in 1 carton / 28 g in 1 tube of First Aid Triple Antibiotic And Pain Relief Maximum Strength, labeled by Lifelabs, A Division Of Atico International Usa, Inc.. 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 Lifelabs, A Division Of Atico International Usa, Inc. on November 01, 2010. The current certification is valid through December 31, 2017.

How is this Lifelabs, A Division Of Atico International Usa, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51852010001. 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)
51852-100-01
11-Digit CMS (5-4-2)
51852-0100-01

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