Osstem S Sensitivity Relief Tooth Paste, Dentifrice
NDC Package 87548-010-02

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

Package Information

Osstem S Sensitivity Relief Tooth (potassium nitrate, sodium fluoride) pastes is uses■ Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact.■ Aids in the prevention of dental cavities. This formulation utilizes a paste, dentifrice delivery system. Marketed by Osstem Pharma Co., Ltd, this product is identified by NDC 87548-010 and is authorized under FDA application M022.

Identification & Billing

NDC Package Code
87548-010-02
Package Description
1 TUBE in 1 CARTON / 120 g in 1 TUBE (87548-010-01)
Product Code
87548-010
11-Digit Billing Format
87548001002
RxNorm Crosswalk
  • RxCUI: 2741131 - potassium nitrate 5 % / sodium fluoride 0.221 % (fluoride ion 0.10 % ) Toothpaste
  • RxCUI: 2741131 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.00221 MG/MG Toothpaste
  • RxCUI: 2741131 - K+ nitrate 0.05 MG/MG / sodium fluoride 0.00221 MG/MG Toothpaste
  • RxCUI: 2741131 - Pot nitrate 0.05 MG/MG / sodium fluoride 0.00221 MG/MG Toothpaste

Clinical Specifications

Proprietary Name
Osstem S Sensitivity Relief Tooth
Non-Proprietary Name
Potassium Nitrate, Sodium Fluoride
Substance Name
Potassium Nitrate; Sodium Fluoride
Dosage Form
Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.
Administration Route
Oral - Administration to or by way of the mouth.
Active Ingredient(s)
Usage Information
Uses■ Builds increasing protection against painful sensitivity of the teeth to cold, heat, acids, sweets or contact.■ Aids in the prevention of dental cavities

Regulatory & Marketing

Labeler Name
Osstem Pharma Co., Ltd
Product Type
Human Otc Drug
FDA Application #
M022
Marketing Category
OTC MONOGRAPH DRUG -
Start Marketing Date
04-01-2026
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 87548-010-02 identifies a specific commercial package of 1 tube in 1 carton / 120 g in 1 tube (87548-010-01) of Osstem S Sensitivity Relief Tooth, a human over the counter drug labeled by Osstem Pharma Co., Ltd. This paste, dentifrice is formulated for oral 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 Osstem Pharma Co., Ltd on April 01, 2026. The current certification is valid through December 31, 2027.

How is this Osstem Pharma Co., Ltd product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 87548001002. 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)
87548-010-02
11-Digit CMS (5-4-2)
87548-0010-02

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