Rematex
NDC Package 69379-002-03

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.

Rematex is iNDICATIONS For the temporary relief of minor pain of muscles and joints associated with: ArthritisSimple Backache Strains Sprains BruisesDIRECTIONSAdults and children over 18 years:Apply generously to affected areaMassage into painful area until thoroughly absorbed into skinRepeat as necessary, not more than 3-4 times daily.Wash hands with soap and water immediately after use.Children 18 years or younger: ask a doctorStore at 20°-25°C (68°-77 °F). Marketed by Home Aide Diganostics, Inc., this product is identified by NDC 69379-002.

Identification & Billing

NDC Package Code
69379-002-03
Package Description
120 g in 1 BOTTLE
Product Code
69379-002
11-Digit Billing Format
69379000203
RxNorm Crosswalk
  • RxCUI: 1655506 - capsaicin 0.035 % / menthol 6 % / methyl salicylate 30 % Topical Cream
  • RxCUI: 1655506 - capsaicin 0.35 MG/ML / menthol 60 MG/ML / methyl salicylate 300 MG/ML Topical Cream

Clinical Specifications

Proprietary Name
Rematex
Dosage Form
-
Usage Information
INDICATIONS For the temporary relief of minor pain of muscles and joints associated with: ArthritisSimple Backache Strains Sprains BruisesDIRECTIONSAdults and children over 18 years:Apply generously to affected areaMassage into painful area until thoroughly absorbed into skinRepeat as necessary, not more than 3-4 times daily.Wash hands with soap and water immediately after use.Children 18 years or younger: ask a doctorStore at 20°-25°C (68°-77 °F). Avoid direct sunlight.

Regulatory & Marketing

Labeler Name
Home Aide Diganostics, Inc.
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
07-10-2015
Listing Expiration
12-31-2017
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 69379-002-03 identifies a specific commercial package of 120 g in 1 bottle of Rematex, labeled by Home Aide Diganostics, 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 Home Aide Diganostics, Inc. on July 10, 2015. The current certification is valid through December 31, 2017.

How is this Home Aide Diganostics, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 69379000203. 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)
69379-002-03
11-Digit CMS (5-4-2)
69379-0002-03

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