Sanamax Menthol Pain Relief Cream
NDC Package 72425-210-03

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.

Sanamax Menthol Pain Relief Cream is uses: temporarily relieves the minor aches and pains of muscles andjoints associated with:  ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains. Marketed by Sanamax Plus Llc, this product is identified by NDC 72425-210 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
72425-210-03
Package Description
100 mL in 1 TUBE
Product Code
72425-210
11-Digit Billing Format
72425021003

Clinical Specifications

Proprietary Name
Sanamax Menthol Pain Relief Cream Cbd
Dosage Form
-
Usage Information
Uses: temporarily relieves the minor aches and pains of muscles andjoints associated with:  ■ simple backache ■ arthritis ■ strains ■ bruises ■ sprains

Regulatory & Marketing

Labeler Name
Sanamax Plus Llc
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
05-31-2022
Listing Expiration
12-31-2025
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 72425-210-03 identifies a specific commercial package of 100 ml in 1 tube of Sanamax Menthol Pain Relief Cream Cbd, labeled by Sanamax Plus Llc. 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 Sanamax Plus Llc on May 31, 2022. The current certification is valid through December 31, 2025.

How is this Sanamax Plus Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72425021003. 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)
72425-210-03
11-Digit CMS (5-4-2)
72425-0210-03

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