Triple Antibiotic
NDC Package 82199-531-13

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Triple Antibiotic is first aid to help prevent infection and for the temporary relief of pain or discomfort in minor: • cuts • scrapes • burns. Marketed by Shandong Ruian Pharmaceutical Co.,ltd., this product is identified by NDC 82199-531 and is authorized under FDA application part333B.

Identification & Billing

NDC Package Code
82199-531-13
Package Description
14.2 g in 1 TUBE
Product Code
11-Digit Billing Format
82199053113
RxNorm Crosswalk
  • RxCUI: 2281302 - bacitracin 500 UNT / lidocaine HCl 40 MG / neomycin 3.5 MG / polymyxin B 5,000 UNT per GM Topical Ointment
  • RxCUI: 2281302 - bacitracin 0.5 UNT/MG / lidocaine hydrochloride 0.04 MG/MG / neomycin 0.0035 MG/MG / polymyxin B 5 UNT/MG Topical Ointment

Clinical Specifications

Proprietary Name
Triple Antibiotic
Dosage Form
-
Usage Information
First aid to help prevent infection and for the temporary relief of pain or discomfort in minor: • cuts • scrapes • burns

Regulatory & Marketing

Labeler Name
Shandong Ruian Pharmaceutical Co.,ltd.
FDA Application #
part333B
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
11-18-2021
Listing Expiration
12-31-2022
Exclude Flag
I
Sample Package
No

Hierarchy Structure

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 (82199-531). Click a package code to view its specific billing and regulatory data.

28.3 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 82199-531-13 identifies a specific commercial package of 14.2 g in 1 tube of Triple Antibiotic, labeled by Shandong Ruian Pharmaceutical 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 Shandong Ruian Pharmaceutical Co.,ltd. on November 18, 2021. The current certification is valid through December 31, 2022.

How is this Shandong Ruian Pharmaceutical Co.,ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 82199053113. 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)
82199-531-13
11-Digit CMS (5-4-2)
82199-0531-13

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