Curetech Chest Rub
NDC Package 73622-3022-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings

Package Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.

Curetech Chest Rub is see important warnings under " When using this product" adults and children 2 years and overrub a thick layer on throat & chest &cover with a warm, dry cloth if desiredkeep clothing loose about throat and chest to help vapors reach the nose and mouthuse up to three times daily or as directed by doctorfor muscle/joint minor aches and pains apply to affected area not more than 3 to 4 times dailychildren under 2 years: do not use. Marketed by Curetech Skincare, this product is identified by NDC 73622-3022 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
73622-3022-1
Package Description
113 g in 1 JAR
Product Code
11-Digit Billing Format
73622302201
RxNorm Crosswalk
  • RxCUI: 2003749 - camphor 4.7 % / eucalyptus oil 1.2 % / menthol 1.25 % Topical Ointment
  • RxCUI: 2003749 - camphor 0.047 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.0125 MG/MG Topical Ointment

Clinical Specifications

Proprietary Name
Curetech Chest Rub
Dosage Form
-
Usage Information
See important warnings under " When using this product" adults and children 2 years and overrub a thick layer on throat & chest &cover with a warm, dry cloth if desiredkeep clothing loose about throat and chest to help vapors reach the nose and mouthuse up to three times daily or as directed by doctorfor muscle/joint minor aches and pains apply to affected area not more than 3 to 4 times dailychildren under 2 years: do not use

Regulatory & Marketing

Labeler Name
Curetech Skincare
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
04-05-2019
Listing Expiration
12-31-2022
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 73622-3022-1 identifies a specific commercial package of 113 g in 1 jar of Curetech Chest Rub, labeled by Curetech Skincare. 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 Curetech Skincare on April 05, 2019. The current certification is valid through December 31, 2022.

How is this Curetech Skincare product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 73622302201. 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 (5-4-1)
73622-3022-1
11-Digit CMS (5-4-2)
73622-3022-01

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