Crest Paste, Dentifrice
NDC Package 69423-784-03
Package Information
Crest (stannous fluoride) pastes is adults and children 12 yrs. This formulation utilizes a paste, dentifrice delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 69423-784 and is authorized under FDA application M021.
Identification & Billing
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.16 % ) Toothpaste
- RxCUI: 416784 - stannous fluoride 0.00454 MG/MG Toothpaste
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416784 - stannous fluoride 0.454 % (fluoride ion 0.15 % ) Toothpaste
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 69423 - The Procter & Gamble Manufacturing Company
- 69423-784 - Crest
- 69423-784-03 - 3 CARTON in 1 CELLO PACK / 1 TUBE in 1 CARTON / 121 g in 1 TUBE
- 69423-784 - Crest
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 (69423-784). Click a package code to view its specific billing and regulatory data.
* 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 69423-784-03 identifies a specific commercial package of 3 carton in 1 cello pack / 1 tube in 1 carton / 121 g in 1 tube of Crest Pro Health With A Touch Of Scope, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. This paste, dentifrice is formulated for dental use and contains stannous 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 The Procter & Gamble Manufacturing Company on October 03, 2022. The current certification is valid through December 31, 2027.
How is this The Procter & Gamble Manufacturing Company product billed for insurance claims?
For medical billing and reimbursement, this package follows the 11-digit CMS format: 69423078403. 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.