No Touch Chest Rub
NDC Package 41250-702-02

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.

No Touch Chest Rub is see important warnings under "When using this product." Remove cap and twist up tube. Marketed by Meijer, this product is identified by NDC 41250-702 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
41250-702-02
Package Description
43 g in 1 TUBE
Product Code
41250-702
11-Digit Billing Format
41250070202
RxNorm Crosswalk
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Topical Ointment
  • RxCUI: 727137 - camphor 0.048 MG/MG / Eucalyptus oil 0.012 MG/MG / menthol 0.026 MG/MG Topical Ointment
  • RxCUI: 727137 - camphor 4.8 % / eucalyptus oil 1.2 % / menthol 2.6 % Chest Rub

Clinical Specifications

Proprietary Name
No Touch Chest Rub
Dosage Form
-
Usage Information
See important warnings under "When using this product." Remove cap and twist up tube. ■ adults and children 2 years and over: ■ rub a thick layer on chest and throat or rub on sore aching muscles ■ cover loosely with a warm, dry cloth, if desired ■ keep clothing loose about throat/chest to help vapors reach the nose/mouth ■ repeat up to three times per 24 hours or as directed by doctor ■ children under 2 years do not use.

Regulatory & Marketing

Labeler Name
Meijer
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
06-01-2016
Listing Expiration
12-31-2019
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 41250-702-02 identifies a specific commercial package of 43 g in 1 tube of No Touch Chest Rub, labeled by Meijer. 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 Meijer on June 01, 2016. The current certification is valid through December 31, 2019.

How is this Meijer product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 41250070202. 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)
41250-702-02
11-Digit CMS (5-4-2)
41250-0702-02

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