Vapour Rub
NDC Package 69729-101-12

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.

Vapour Rub is aDULTS AND CHILDREN 2 YEARS AND OVER:FOR COUGH SUPPRESSIONRUB A THICK LAYER ON THROAT & CHESTCOVER 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 A 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 Opmx Llc, this product is identified by NDC 69729-101 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
69729-101-12
Package Description
1 JAR in 1 BOX / 50 g in 1 JAR
Product Code
11-Digit Billing Format
69729010112
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
Vapour Rub
Dosage Form
-
Usage Information
ADULTS AND CHILDREN 2 YEARS AND OVER:FOR COUGH SUPPRESSIONRUB A THICK LAYER ON THROAT & CHESTCOVER 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 A 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
Opmx Llc
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
07-16-2018
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (69729-101). Click a package code to view its specific billing and regulatory data.

1 JAR in 1 BOX / 100 g in 1 JAR

* 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 69729-101-12 identifies a specific commercial package of 1 jar in 1 box / 50 g in 1 jar of Vapour Rub, labeled by Opmx 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 Opmx Llc on July 16, 2018. The current certification is valid through December 31, 2019.

How is this Opmx Llc product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69729010112. 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)
69729-101-12
11-Digit CMS (5-4-2)
69729-0101-12

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