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  5. NDC Package Code: 60258-151-01 Sf

NDC Package 60258-151-01 Sf

1.1% Sodium Fluoride Gel Dental - View Billable Units, 11-Digit Format, RxNorm

Table of Contents

    1. Package Information
    2. Frequently Asked Questions

Package Information

Find all the important details about this NDC Package code, including the 11-Digit NDC Billing number, billing units, wholesale price, RxNorm crosswalk, active ingredients, pharmacologic clasess, etc.

NDC Package Code:
60258-151-01
Package Description:
1 TUBE in 1 CARTON / 56 g in 1 TUBE
Product Code:
60258-151
Proprietary Name:
Sf
Non-Proprietary Name:
1.1% Sodium Fluoride
Substance Name:
Sodium Fluoride
Usage Information:
This medication is used to prevent cavities. It makes teeth stronger and more resistant to decay caused by acid and bacteria.
11-Digit NDC Billing Format:
60258015101
Billing Unit:
GM - Billing unit of "gram" is used when a product is measured by its weight.
NDC to RxNorm Crosswalk:
56 GM
NDC to RxNorm Crosswalk:
  • RxCUI: 392038 - sodium fluoride 1.1 % Toothpaste
  • RxCUI: 392038 - sodium fluoride 0.011 MG/MG Toothpaste
  • RxCUI: 392038 - sodium fluoride 1.1 % (fluoride ion 0.5 % ) Toothpaste
  • RxCUI: 392038 - sodium fluoride 1.1 % Dental Gel
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Cypress Pharmaceutical, Inc.
    Dosage Form:
    Gel - A semisolid3 dosage form that contains a gelling agent to provide stiffness to a solution or a colloidal dispersion.4 A gel may contain suspended particles.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
    • Active Ingredient(s):
  • SODIUM FLUORIDE 11 mg/g
    • Sample Package:
    No
    Marketing Category:
    UNAPPROVED DRUG OTHER - An unapproved drug product in a marketing category that is not reflected on a particular list.
    Start Marketing Date:
    12-01-1999
    Listing Expiration Date:
    12-31-2024
    Exclude Flag:
    N
    Code Structure:

    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 disclaimer below.

    Frequently Asked Questions

    What is NDC 60258-151-01?

    The NDC Packaged Code 60258-151-01 is assigned to a package of 1 tube in 1 carton / 56 g in 1 tube of Sf, a human prescription drug labeled by Cypress Pharmaceutical, Inc.. The product's dosage form is gel and is administered via dental form.

    Is NDC 60258-151 included in the NDC Directory?

    Yes, Sf with product code 60258-151 is active and included in the NDC Directory. The product was first marketed by Cypress Pharmaceutical, Inc. on December 01, 1999 and its listing in the NDC Directory is set to expire on December 31, 2024 if the product is not updated or renewed by the manufacturer.

    What is the NDC billing unit for package 60258-151-01?

    The contents of this package are billed per "gm or gram", products billed per gram are products measured by weight. The calculated billable units for this package is 56.

    What is the 11-digit format for NDC 60258-151-01?

    The 11-digit format is 60258015101. The 11-digit billing format might be required by the Centers for Medicare & Medicaid Services (CMS) and other payers in billing claim forms.

    This package code is originally configured in a 5-3-2 segment 10-digit format and by adding a zero within the original NDC package code we can obtain the converted 11-digit format in a 5-4-2 segment configuration. The table below shows the 11-digit code conversion:

    10-Digit Format10-Digit Original Code11-Digit Format11-Digit Code
    5-3-260258-151-015-4-260258-0151-01