Anticavity Mouth Rinse Low-foaming Spearmint Mouthwash
NDC Package 87649-7180-1

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 (718 us variant anticavity mouth rinse low-foaming spearmint) mouthwashes is directions Adults and children 6 years of age and older Use twice a day after brushing your teeth with a toothpaste. This formulation utilizes a mouthwash delivery system. Marketed by Dyson Technology Limited, this product is identified by NDC 87649-7180 and is authorized under FDA application M021.

Identification & Billing

NDC Package Code
87649-7180-1
Package Description
400 mL in 1 BOTTLE
Product Code
87649-7180
11-Digit Billing Format
87649718001

Clinical Specifications

Proprietary Name
Anticavity Mouth Rinse Low-foaming Spearmint
Non-Proprietary Name
718 Us Variant Anticavity Mouth Rinse Low-foaming Spearmint
Substance Name
Sodium Fluoride
Dosage Form
Mouthwash - An aqueous solution which is most often used for its deodorant, refreshing, or antiseptic effect.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
SODIUM FLUORIDE .02 g/100mL
Usage Information
Directions Adults and children 6 years of age and older Use twice a day after brushing your teeth with a toothpaste. • vigorously swish 10 millilitres 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.

Regulatory & Marketing

Labeler Name
Dyson Technology Limited
Product Type
Human Otc Drug
FDA Application #
M021
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
06-10-2026
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 87649-7180-1 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 mouthwash 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 June 10, 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: 87649718001. 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)
87649-7180-1
11-Digit CMS (5-4-2)
87649-7180-01

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