Crest Deep Cleanse Rinse
NDC Package 84126-607-16
Package Information
Crest Deep Cleanse (sodium fluoride) rinses is adults and children 6 years & older: Use twice a day after brushing your teeth with a toothpaste.Vigorously swish 10 mL of rinse between your teeth for 1 minute and then spit out.Do not swallow the rinse.Do not eat or drink for 30 minutes after rinsing.Instruct children under 12 years of age in good rinsing habits (to minimize swallowing).Supervise children as necessary until capable of using without supervision.Children under 6 years of age: consult a dentist or doctor. This formulation utilizes a rinse delivery system. Marketed by The Procter & Gamble Manufacturing Company, this product is identified by NDC 84126-607 and is authorized under FDA application M021.
Identification & Billing
- RxCUI: 1658137 - Crest 0.02 % Mouthwash
- RxCUI: 1658137 - sodium fluoride 0.2 MG/ML Mouthwash [Crest]
- RxCUI: 1658137 - Crest 0.0219 % (fluoride ion 0.01 % ) Oral Rinse
- RxCUI: 1658137 - Crest 0.2 MG/ML Mouthwash
- RxCUI: 1658137 - Crest Pro-Health Advanced 0.02 % (0.01 % fluoride ion) Mouthwash
Clinical Specifications
Regulatory & Marketing
Hierarchy Structure
- 84126 - The Procter & Gamble Manufacturing Company
- 84126-607 - Crest Deep Cleanse
- 84126-607-16 - 475 mL in 1 BOTTLE, PLASTIC
- 84126-607 - Crest Deep Cleanse
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 84126-607-16 identifies a specific commercial package of 475 ml in 1 bottle, plastic of Crest Deep Cleanse Cavity Defense, a human over the counter drug labeled by The Procter & Gamble Manufacturing Company. This rinse 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 The Procter & Gamble Manufacturing Company on January 01, 2024. 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: 84126060716. 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.