Therabreath Fresh Breath Anticavity Mild Mint Paste, Dentifrice
NDC Package 10237-263-04
Package Information
Therabreath Fresh Breath Anticavity Mild Mint (sodium fluoride) pastes is do not swallow.Supervise children as necessary until capable of using without supervision.Adults and children 6 years of age and older: Brush teeth thoroughly, preferably after each meal or at least twice a day, or as directed by a dentist or doctor. This formulation utilizes a paste, dentifrice delivery system. Marketed by Church & Dwight Co., Inc., this product is identified by NDC 10237-263 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
- 10237 - Church & Dwight Co., Inc.
- 10237-263 - Therabreath Fresh Breath Anticavity Mild Mint
- 10237-263-04 - 1 TUBE in 1 CARTON / 113.5 g in 1 TUBE
- 10237-263 - Therabreath Fresh Breath Anticavity Mild Mint
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.
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Frequently Asked Questions
What is the distribution configuration for this product package?
The code 10237-263-04 identifies a specific commercial package of 1 tube in 1 carton / 113.5 g in 1 tube of Therabreath Fresh Breath Anticavity Mild Mint, a human over the counter drug labeled by Church & Dwight Co., Inc.. This paste, dentifrice is formulated for oral 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 Church & Dwight Co., Inc. on February 08, 2024. The current certification is valid through December 31, 2026.
How is this Church & Dwight Co., Inc. product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 10237026304. 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.