Mipaste
NDC Package 61596-882-41

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 discontinued by the firm.

Mipaste is * Adults and children over 12: brush teeth with your normal toothpaste at least twice a day, or as directed by your dental profession or doctor, rinse mouth after brushing, dispense a pea-sized portion of MI Paste Plus onto your finger, apply thoroughly, coating the upper teeth with an even layer, repeat for lower teeth, allow to remain on teeth for 3 mintues. Marketed by Gc America Inc., this product is identified by NDC 61596-882 and is authorized under FDA application M021.

Identification & Billing

NDC Package Code
61596-882-41
Package Description
1 TUBE in 1 BOX / 40 g in 1 TUBE (61596-882-40)
Product Code
61596-882
11-Digit Billing Format
61596088241
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Mipaste Plus
Dosage Form
-
Usage Information
* Adults and children over 12: brush teeth with your normal toothpaste at least twice a day, or as directed by your dental profession or doctor, rinse mouth after brushing, dispense a pea-sized portion of MI Paste Plus onto your finger, apply thoroughly, coating the upper teeth with an even layer, repeat for lower teeth, allow to remain on teeth for 3 mintues. Do not rinse.* Children under the age of 12: consult your dental professional or doctor.

Regulatory & Marketing

Labeler Name
Gc America Inc.
FDA Application #
M021
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-01-2015
End Marketing Date
12-31-2025
Listing Expiration
12-31-2025
Exclude Flag
D
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 61596-882-41 identifies a specific commercial package of 1 tube in 1 box / 40 g in 1 tube (61596-882-40) of Mipaste Plus, labeled by Gc America 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 Gc America Inc. on June 01, 2015. The current certification is valid through December 31, 2025.

How is this Gc America Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 61596088241. 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)
61596-882-41
11-Digit CMS (5-4-2)
61596-0882-41

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