Lusti Profesional Vaporizing Rub
NDC Package 49681-012-03

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.

Lusti Profesional Vaporizing Rub is see important warnings under "When using this product". Marketed by New Life Products, Inc., this product is identified by NDC 49681-012 and is authorized under FDA application part341.

Identification & Billing

NDC Package Code
49681-012-03
Package Description
113 g in 1 JAR
Product Code
49681-012
11-Digit Billing Format
49681001203
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
Lusti Profesional Vaporizing Rub
Dosage Form
-
Usage Information
See important warnings under "When using this product". Adults and children 2 years and older, rub on throat and chest in a thick layer.  Cover with a warm dry cloth if desired.  Clothing should be loose about throat and chest to help vapors reach the nose and mouth.  Use up to three times daily or as directed by a doctor.  Children under 2 years of age: Ask a doctor.

Regulatory & Marketing

Labeler Name
New Life Products, Inc.
FDA Application #
part341
Marketing Category
OTC MONOGRAPH FINAL - A product marketed pursuant to a final Over-the-Counter (OTC) Drug Monograph.
Start Marketing Date
08-04-2010
Listing Expiration
12-31-2024
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 49681-012-03 identifies a specific commercial package of 113 g in 1 jar of Lusti Profesional Vaporizing Rub, labeled by New Life Products, Inc.. 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 New Life Products, Inc. on August 04, 2010. The current certification is valid through December 31, 2024.

How is this New Life Products, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49681001203. 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)
49681-012-03
11-Digit CMS (5-4-2)
49681-0012-03

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