Anti-bacterial Foaming
NDC Package 49852-005-08

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.

Anti-bacterial Foaming is wet hands, work into a lather. Marketed by Tri-coastal Design Company Inc., this product is identified by NDC 49852-005 and is authorized under FDA application part333A.

Identification & Billing

NDC Package Code
49852-005-08
Package Description
240 mL in 1 BOTTLE, PUMP
Product Code
49852-005
11-Digit Billing Format
49852000508
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Anti-bacterial Foaming
Dosage Form
-
Usage Information
Wet hands, work into a lather. Rinse wellsupervise children in the use of this productin the case of eye contact, rinse eyes thoroughly with water

Regulatory & Marketing

Labeler Name
Tri-coastal Design Company Inc.
FDA Application #
part333A
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
08-15-2011
Listing Expiration
12-31-2018
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 49852-005-08 identifies a specific commercial package of 240 ml in 1 bottle, pump of Anti-bacterial Foaming, labeled by Tri-coastal Design Company 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 Tri-coastal Design Company Inc. on August 15, 2011. The current certification is valid through December 31, 2018.

How is this Tri-coastal Design Company Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 49852000508. 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)
49852-005-08
11-Digit CMS (5-4-2)
49852-0005-08

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