Point Relief Cold Spot Pain Relieving Roll-on Liquid
NDC Package 51452-037-06

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Point Relief Cold Spot Pain Relieving Roll-on (menthol) liquids is apply directly to affected area. This formulation utilizes a liquid delivery system. Marketed by Fabrication Enterprises, this product is identified by NDC 51452-037 and is authorized under FDA application M017.

Identification & Billing

NDC Package Code
51452-037-06
Package Description
90 mL in 1 CONTAINER
Product Code
51452-037
11-Digit Billing Format
51452003706
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Point Relief Cold Spot Pain Relieving Roll-on
Non-Proprietary Name
Menthol
Substance Name
Menthol
Dosage Form
Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.
Administration Route
Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
Active Ingredient(s)
MENTHOL 140 mg/mL
Usage Information
Apply directly to affected area. Do not use more than four fimes per day.

Regulatory & Marketing

Labeler Name
Fabrication Enterprises
Product Type
Human Otc Drug
FDA Application #
M017
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2019
Listing Expiration
12-31-2026
Exclude Flag
N
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 51452-037-06 identifies a specific commercial package of 90 ml in 1 container of Point Relief Cold Spot Pain Relieving Roll-on, a human over the counter drug labeled by Fabrication Enterprises. This liquid is formulated for topical use and contains menthol as the active substance.

Is this product currently listed with the FDA?

Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Fabrication Enterprises on April 01, 2019. The current certification is valid through December 31, 2026.

How is this Fabrication Enterprises product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 51452003706. 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)
51452-037-06
11-Digit CMS (5-4-2)
51452-0037-06

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