Fluoride Anticavity,toothpaste Paste, Dentifrice
NDC Package 87576-332-02

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

Package Information

Fluoride Anticavity, Toothpaste pastes is it is recommended to brush your teeth after each meal or at least twice a day. This formulation utilizes a paste, dentifrice delivery system. Marketed by Shulisa (foshan) Daily Chemicalindustry Co., Ltd, this product is identified by NDC 87576-332.

Identification & Billing

NDC Package Code
87576-332-02
Package Description
1 TUBE in 1 BOX / 1 PASTE, DENTIFRICE in 1 TUBE
Product Code
87576-332
11-Digit Billing Format
87576033202
RxNorm Crosswalk
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )Toothpaste

Clinical Specifications

Proprietary Name
Fluoride Anticavity, Toothpaste
Non-Proprietary Name
Fluoride Anticavity Toothpaste
Substance Name
Sodium Monofluorophosphate
Dosage Form
Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.
Administration Route
Dental - Administration to a tooth or teeth.
Active Ingredient(s)
SODIUM MONOFLUOROPHOSPHATE .76 g/1
Usage Information
It is recommended to brush your teeth after each meal or at least twice a day.

Regulatory & Marketing

Labeler Name
Shulisa (foshan) Daily Chemicalindustry Co., Ltd
Product Type
Human Otc Drug
Marketing Category
UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
Start Marketing Date
04-03-2026
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 87576-332-02 identifies a specific commercial package of 1 tube in 1 box / 1 paste, dentifrice in 1 tube of Fluoride Anticavity, Toothpaste, a human over the counter drug labeled by Shulisa (foshan) Daily Chemicalindustry Co., Ltd. This paste, dentifrice is formulated for dental use and contains sodium monofluorophosphate 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 Shulisa (foshan) Daily Chemicalindustry Co., Ltd on April 03, 2026. The current certification is valid through December 31, 2027.

How is this Shulisa (foshan) Daily Chemicalindustry Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87576033202. 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)
87576-332-02
11-Digit CMS (5-4-2)
87576-0332-02

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