Bacitracin Zinc
NDC Package 67777-239-01

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.

Bacitracin Zinc is indications and UsageFor first aid to help prevent infection in minor skin abrasions and rashes. Marketed by Dynarex Corporation, this product is identified by NDC 67777-239 and is authorized under FDA application part333B.

Identification & Billing

NDC Package Code
67777-239-01
Package Description
12 BOX in 1 CASE / 144 PACKET in 1 BOX / .9 g in 1 PACKET
Product Code
67777-239
11-Digit Billing Format
67777023901
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Bacitracin Zinc
Dosage Form
-
Usage Information
Indications and UsageFor first aid to help prevent infection in minor skin abrasions and rashes.

Regulatory & Marketing

Labeler Name
Dynarex Corporation
FDA Application #
part333B
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
12-01-2009
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 67777-239-01 identifies a specific commercial package of 12 box in 1 case / 144 packet in 1 box / .9 g in 1 packet of Bacitracin Zinc, labeled by Dynarex Corporation. 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 Dynarex Corporation on December 01, 2009. The current certification is valid through December 31, 2017.

How is this Dynarex Corporation product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 67777023901. 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)
67777-239-01
11-Digit CMS (5-4-2)
67777-0239-01

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