Seavue Dental Desensitizer Gel, Dentifrice
NDC Package 87118-003-01

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

Package Information

Seavue Dental Desensitizer (potassium nitrate and sodium fluoride dentifrice) gel is adults and children 12 years and older:Apply the product using one of the following methods:Apply evenly on a mouthguard, wear for 15–30 minutes, then remove and rinse. This formulation utilizes a gel, dentifrice delivery system. Marketed by Xiling (zhenjiang) Medical Technology Co., Ltd., this product is identified by NDC 87118-003 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
87118-003-01
Package Description
1 g in 1 BOX
Product Code
87118-003
11-Digit Billing Format
87118000301

Clinical Specifications

Proprietary Name
Seavue Dental Desensitizer
Non-Proprietary Name
Potassium Nitrate And Sodium Fluoride Dentifrice
Substance Name
Potassium Nitrate; 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
Dental - Administration to a tooth or teeth.
Active Ingredient(s)
Usage Information
Adults and children 12 years and older:Apply the product using one of the following methods:Apply evenly on a mouthguard, wear for 15–30 minutes, then remove and rinse. Or apply directly to sensitive teeth using a cotton swab or soft brush. Rub gently, leave for 2–3 minutes, rinse and spit out. Use once or twice daily as needed.Children under 12 years: ask a dentist.

Regulatory & Marketing

Labeler Name
Xiling (zhenjiang) Medical Technology Co., Ltd.
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
10-08-2025
Listing Expiration
12-31-2026
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 87118-003-01 identifies a specific commercial package of 1 g in 1 box of Seavue Dental Desensitizer, a human over the counter drug labeled by Xiling (zhenjiang) Medical Technology Co., Ltd.. This gel, dentifrice is formulated for dental use and contains potassium nitrate; 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 Xiling (zhenjiang) Medical Technology Co., Ltd. on October 08, 2025. The current certification is valid through December 31, 2026.

How is this Xiling (zhenjiang) Medical Technology Co., Ltd. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87118000301. 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 (5-3-2)
87118-003-01
11-Digit CMS (5-4-2)
87118-0003-01

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