Triple Antibiotic Plus
NDC Package 41250-961-56

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.

Triple Antibiotic Plus is directionsadults and children 2 years of age and older:clean the affected areaapply 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 timesmay be covered with a sterile bandagechildren under 2 years of age: ask a doctor. Marketed by Meijer, Inc., this product is identified by NDC 41250-961 and is authorized under FDA application part333B.

Identification & Billing

NDC Package Code
41250-961-56
Package Description
2 TUBE in 1 CARTON / 28 g in 1 TUBE
Product Code
41250-961
11-Digit Billing Format
41250096156
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
Triple Antibiotic Plus
Dosage Form
-
Usage Information
Directionsadults and children 2 years of age and older:clean the affected areaapply 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 timesmay be covered with a sterile bandagechildren under 2 years of age: ask a doctor

Regulatory & Marketing

Labeler Name
Meijer, 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
12-18-2018
Listing Expiration
12-31-2021
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 (41250-961). Click a package code to view its specific billing and regulatory data.

41250-961-14
1 TUBE in 1 CARTON / 14 g in 1 TUBE
41250-961-28
1 TUBE in 1 CARTON / 28 g in 1 TUBE

* 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 41250-961-56 identifies a specific commercial package of 2 tube in 1 carton / 28 g in 1 tube of Triple Antibiotic Plus, labeled by Meijer, 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 Meijer, Inc. on December 18, 2018. The current certification is valid through December 31, 2021.

How is this Meijer, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41250096156. 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)
41250-961-56
11-Digit CMS (5-4-2)
41250-0961-56

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