Derma-glove
NDC Package 24673-249-01

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.

Derma-glove is hand sanitizer to help reduce bacteria on the skin that could cause diseaseRecommended for repeated use. Marketed by Rwm Technologies, this product is identified by NDC 24673-249 and is authorized under FDA application part333.

Identification & Billing

NDC Package Code
24673-249-01
Package Description
13.65 g in 1 BOTTLE, SPRAY
Product Code
11-Digit Billing Format
24673024901
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Derma-glove
Dosage Form
-
Usage Information
Hand sanitizer to help reduce bacteria on the skin that could cause diseaseRecommended for repeated use

Regulatory & Marketing

Labeler Name
Rwm Technologies
FDA Application #
part333
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
02-03-2010
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.

Other Available Packages

The following commercial packages are registered under the same Product NDC (24673-249). Click a package code to view its specific billing and regulatory data.

3494.4 g in 1 BOTTLE, SPRAY
17472 g in 1 DRUM
192192 g in 1 DRUM
873600 g in 1 DRUM
1223040 g in 1 DRUM

* 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 24673-249-01 identifies a specific commercial package of 13.65 g in 1 bottle, spray of Derma-glove, labeled by Rwm Technologies. 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 Rwm Technologies on February 03, 2010. The current certification is valid through December 31, 2017.

How is this Rwm Technologies product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 24673024901. 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)
24673-249-01
11-Digit CMS (5-4-2)
24673-0249-01

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