Mipaste One Kids Bubble Gum Paste, Dentifrice
NDC Package 61596-101-10
Package Information
Mipaste One Kids Bubble Gum pastes is use - aids in the prevention of dental cavities Anti-cavity toothpaste with bio-available calcium, phosphate and Fluoride. This formulation utilizes a paste, dentifrice delivery system. Marketed by Gc America Inc., this product is identified by NDC 61596-101 and is authorized under FDA application M021.
Identification & Billing
- RxCUI: 416783 - sodium fluoride 0.24 % Toothpaste
- RxCUI: 416783 - sodium fluoride 0.0024 MG/MG Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.15 % ) Toothpaste
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 61596 - Gc America Inc.
- 61596-101 - Mipaste One Kids Bubble Gum
- 61596-101-10 - 10 BOX, UNIT-DOSE in 1 BOX / 1 TUBE in 1 BOX, UNIT-DOSE (61596-101-02) / 46 g in 1 TUBE (61596-101-01)
- 61596-101 - Mipaste One Kids Bubble Gum
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 61596-101-10 identifies a specific commercial package of 10 box, unit-dose in 1 box / 1 tube in 1 box, unit-dose (61596-101-02) / 46 g in 1 tube (61596-101-01) of Mipaste One Kids Bubble Gum, a human over the counter drug labeled by Gc America Inc.. This paste, dentifrice is formulated for dental use and contains sodium fluoride as the active substance.
Is this product currently listed with the FDA?
Yes, this product is active and verified within the NDC Directory. It was introduced to the market by Gc America Inc. on April 21, 2021. The current certification is valid through December 31, 2026.
How is this Gc America Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 61596010110. 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:
Note: The zero is added to the Product segment to maintain the 5-4-2 structure.