Banish My Pain
NDC Package 72895-081-02

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.

Banish My Pain is adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.massage into area until thoroughly absorbedChildren under 2 years of age: consult a doctor. Marketed by Laiden Montana Emu Products, this product is identified by NDC 72895-081 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
72895-081-02
Package Description
60 mL in 1 JAR
Product Code
72895-081
11-Digit Billing Format
72895008102

Clinical Specifications

Proprietary Name
Banish My Pain
Dosage Form
-
Usage Information
Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily.massage into area until thoroughly absorbedChildren under 2 years of age: consult a doctor.

Regulatory & Marketing

Labeler Name
Laiden Montana Emu Products
FDA Application #
part348
Marketing Category
OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
Start Marketing Date
05-06-2019
Listing Expiration
12-31-2020
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 72895-081-02 identifies a specific commercial package of 60 ml in 1 jar of Banish My Pain, labeled by Laiden Montana Emu Products. 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 Laiden Montana Emu Products on May 06, 2019. The current certification is valid through December 31, 2020.

How is this Laiden Montana Emu Products product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72895008102. 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)
72895-081-02
11-Digit CMS (5-4-2)
72895-0081-02

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