Lusti Therapeutic Ice Analgesic Rub
NDC Package 49681-010-10

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 Therapeutic Ice Analgesic Rub is apply liberally to painful area and massage until gel is absorbed into the skin.  Repeat three to four times daily. Marketed by New Life Products, Inc., this product is identified by NDC 49681-010 and is authorized under FDA application part348.

Identification & Billing

NDC Package Code
49681-010-10
Package Description
284 g in 1 JAR
Product Code
49681-010
11-Digit Billing Format
49681001010
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Lusti Therapeutic Ice Analgesic Rub
Dosage Form
-
Usage Information
Apply liberally to painful area and massage until gel is absorbed into the skin.  Repeat three to four times daily.

Regulatory & Marketing

Labeler Name
New Life Products, Inc.
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
03-24-2010
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 49681-010-10 identifies a specific commercial package of 284 g in 1 jar of Lusti Therapeutic Ice Analgesic 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 March 24, 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: 49681001010. 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)
49681-010-10
11-Digit CMS (5-4-2)
49681-0010-10

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