Sf 5000 Plus Cream
NDC Package 60258-150-01

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

Package Information

Sf 5000 Plus (1.1% sodium fluoride prescription dental cream) cream is sodium fluoride makes teeth more resistant to decay and bacteria that cause cavities. This formulation utilizes a cream delivery system. Marketed by Cypress Pharmaceutical, Inc., this product is identified by NDC 60258-150.

Identification & Billing

NDC Package Code
60258-150-01
Package Description
1 TUBE in 1 CARTON / 51 g in 1 TUBE
Product Code
60258-150
11-Digit Billing Format
60258015001
Billing Unit
GM - Billing unit of "gram" is used when a product is measured by its weight.
Units Per Package
51 GM
RxNorm Crosswalk

Clinical Specifications

Proprietary Name
Sf 5000 Plus
Non-Proprietary Name
1.1% Sodium Fluoride Prescription Dental Cream
Substance Name
Sodium Fluoride
Dosage Form
Cream - An emulsion, semisolid3 dosage form, usually containing > 20% water and volatiles5 and/or < 50% hydrocarbons, waxes, or polyols as the vehicle. This dosage form is generally for external application to the skin or mucous membranes.
Administration Route
Dental - Administration to a tooth or teeth.
Active Ingredient(s)
SODIUM FLUORIDE 5 mg/g
Usage Information
Sodium fluoride makes teeth more resistant to decay and bacteria that cause cavities. This medication is used to prevent cavities.

Regulatory & Marketing

Labeler Name
Cypress Pharmaceutical, Inc.
Product Type
Human Prescription 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
11-12-1999
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 60258-150-01 identifies a specific commercial package of 1 tube in 1 carton / 51 g in 1 tube of Sf 5000 Plus, a human prescription drug labeled by Cypress Pharmaceutical, Inc.. This cream is formulated for dental 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 Cypress Pharmaceutical, Inc. on November 12, 1999. The current certification is valid through December 31, 2026.

What are the primary indications for this medication?

Sodium fluoride makes teeth more resistant to decay and bacteria that cause cavities. This medication is used to prevent cavities.

How is this Cypress Pharmaceutical, Inc. product billed for insurance claims?

For medical billing and reimbursement, this package follows the 11-digit CMS format: 60258015001. Quantities are measured in per "gm or gram", products billed per gram are products measured by weight.. There are 51 total billable units per package. 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)
60258-150-01
11-Digit CMS (5-4-2)
60258-0150-01

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