Anticavity Mouth Rinse Low-foaming Spearmint Gel, Dentifrice
NDC Package 87649-0718-1

View Billable Units, 11-Digit Conversion Format, and RxNorm mappings
Table of Contents
    1. Package Information
    2. Frequently Asked Questions

Package Information

Anticavity Mouth Rinse Low-foaming Spearmint (779 us variant anticavity mouth rinse low-foaming spearmint) gel is do not swallow the rinse. This formulation utilizes a gel, dentifrice delivery system. Marketed by Dyson Technology Limited, this product is identified by NDC 87649-0718 and is authorized under FDA application M021.

Identification & Billing

NDC Package Code
87649-0718-1
Package Description
400 mL in 1 BOTTLE
Product Code
87649-0718
11-Digit Billing Format
87649071801

Clinical Specifications

Proprietary Name
Anticavity Mouth Rinse Low-foaming Spearmint
Non-Proprietary Name
779 Us Variant Anticavity Mouth Rinse Low-foaming Spearmint
Substance Name
Sodium Fluoride
Dosage Form
Gel, Dentifrice - A combination of a dentifrice (formulation intended to clean and/or polish the teeth, and which may contain certain additional agents), and a gel. It is used with a toothbrush for the purpose of cleaning and polishing the teeth.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
SODIUM FLUORIDE .02 g/100mL
Usage Information
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

Regulatory & Marketing

Labeler Name
Dyson Technology Limited
Product Type
Human Otc Drug
FDA Application #
M021
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
07-31-2026
Listing Expiration
12-31-2027
Exclude Flag
N
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 87649-0718-1 identifies a specific commercial package of 400 ml in 1 bottle of Anticavity Mouth Rinse Low-foaming Spearmint, a human over the counter drug labeled by Dyson Technology Limited. This gel, 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 Dyson Technology Limited on July 31, 2026. The current certification is valid through December 31, 2027.

How is this Dyson Technology Limited product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87649071801. 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 (5-4-1)
87649-0718-1
11-Digit CMS (5-4-2)
87649-0718-01

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