Cool Breeze
NDC Package 72744-778-40

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.

Cool Breeze is adults and children over 12 years:• Apply generously to affected area.• Massage into painful area until thoroughly absorbed into skin• Repeat as necessary, But no more than 4 times dailyChildren 12 years or younger:• Please speak with a doctor. Marketed by Cool Breeze Us Llc, this product is identified by NDC 72744-778 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
72744-778-40
Package Description
113 g in 1 TUBE
Product Code
72744-778
11-Digit Billing Format
72744077840
RxNorm Crosswalk
  • RxCUI: 2105836 - menthol 5 % / methyl salicylate 4 % Topical Gel
  • RxCUI: 2105836 - menthol 0.05 MG/MG / methyl salicylate 0.04 MG/MG Topical Gel

Clinical Specifications

Proprietary Name
Cool Breeze
Dosage Form
-
Usage Information
Adults and children over 12 years:• Apply generously to affected area.• Massage into painful area until thoroughly absorbed into skin• Repeat as necessary, But no more than 4 times dailyChildren 12 years or younger:• Please speak with a doctor

Regulatory & Marketing

Labeler Name
Cool Breeze Us Llc
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
12-06-2021
Listing Expiration
12-31-2023
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 72744-778-40 identifies a specific commercial package of 113 g in 1 tube of Cool Breeze, labeled by Cool Breeze Us 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 Cool Breeze Us Llc on December 06, 2021. The current certification is valid through December 31, 2023.

How is this Cool Breeze Us Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 72744077840. 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)
72744-778-40
11-Digit CMS (5-4-2)
72744-0778-40

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