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  5. NDC Package Code: 65222-411-32 Nupro Fluorides Naf Oral Solution Mandarin Orange

NDC Package 65222-411-32 Nupro Fluorides Naf Oral Solution Mandarin Orange

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:
65222-411-32
Package Description:
7 g in 1 BOTTLE, PLASTIC
Product Code:
65222-411
Proprietary Name:
Nupro Fluorides Naf Oral Solution Mandarin Orange
Non-Proprietary Name:
Sodium Fluoride
Substance Name:
Sodium Fluoride
Usage Information:
For topical application to aid in the protection against dental caries. The non-acidic fluoride is safe for patients with porcelain, composite restorations, and sealants.
11-Digit NDC Billing Format:
65222041132
NDC to RxNorm Crosswalk:
  • RxCUI: 1993075 - Nupro 2 % Dental Gel
  • RxCUI: 1993075 - sodium fluoride 0.02 MG/MG Oral Gel [NuPro]
  • RxCUI: 1993075 - NuPro 0.02 MG/MG Dental Gel
  • RxCUI: 1993075 - NuPro 2 % (fluoride ion 0.9 % ) Oral Gel
  • RxCUI: 245593 - sodium fluoride 2 % Dental Gel
    • Product Type:
    Human Prescription Drug
    Labeler Name:
    Dentsply Llc. Professional Division Trading As "dentsply Professional"
    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 20 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:
    01-01-1974
    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 65222-411-32?

    The NDC Packaged Code 65222-411-32 is assigned to a package of 7 g in 1 bottle, plastic of Nupro Fluorides Naf Oral Solution Mandarin Orange, a human prescription drug labeled by Dentsply Llc. Professional Division Trading As "dentsply Professional". The product's dosage form is gel and is administered via dental form.

    Is NDC 65222-411 included in the NDC Directory?

    Yes, Nupro Fluorides Naf Oral Solution Mandarin Orange with product code 65222-411 is active and included in the NDC Directory. The product was first marketed by Dentsply Llc. Professional Division Trading As "dentsply Professional" on January 01, 1974 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 11-digit format for NDC 65222-411-32?

    The 11-digit format is 65222041132. 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
    5-3-265222-411-325-4-265222-0411-32