NDC Package 57511-0102-3 Fluorimax 5000 Sensitive

1.1% Sodium Fluoride With 5% Potassium Nitrate Toothpaste Paste, Dentifrice Topical - View Billable Units, 11-Digit Format, RxNorm

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:
57511-0102-3
Package Description:
96 g in 1 TUBE
Product Code:
Proprietary Name:
Fluorimax 5000 Sensitive
Non-Proprietary Name:
1.1% Sodium Fluoride With 5% Potassium Nitrate Toothpaste
Substance Name:
Potassium Nitrate; Sodium Fluoride
Usage Information:
A dental caries preventive and sensitive teeth toothpaste for once daily self appied topical use. It is well established that 1.1% sodium fluoride is safe and effective as a caries preventive when applied frequently with mouthpiece applicators. Use once daily in place of your regular toothpaste unless otherwise instructed by your dental professional.
11-Digit NDC Billing Format:
57511010203
NDC to RxNorm Crosswalk:
  • RxCUI: 2603764 - FluoriMax 5000 Sensitive 5 % / 1.1 % Toothpaste
  • RxCUI: 2603764 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.011 MG/MG Toothpaste [Fluorimax Sensitive]
  • RxCUI: 2603764 - Fluorimax Sensitive (potassium nitrate 5 % / sodium fluoride 1.1 % ) Toothpaste
  • RxCUI: 2603764 - K+ nitrate 0.05 MG/MG / sodium fluoride 0.011 MG/MG Toothpaste [Fluorimax Sensitive]
  • RxCUI: 2603764 - Pot nitrate 0.05 MG/MG / sodium fluoride 0.011 MG/MG Toothpaste [Fluorimax Sensitive]
  • Product Type:
    Human Otc Drug
    Labeler Name:
    Elevate Oral Care
    Dosage Form:
    Paste, Dentifrice - A paste formulation intended to clean and/or polish the teeth, and which may contain certain additional agents.
    Administration Route(s):
  • Topical - Administration to a particular spot on the outer surface of the body. The E2B term TRANSMAMMARY is a subset of the term TOPICAL.
  • 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:
    08-01-2017
    End Marketing Date:
    10-31-2024
    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 57511-0102-3?

    The NDC Packaged Code 57511-0102-3 is assigned to a package of 96 g in 1 tube of Fluorimax 5000 Sensitive, a human over the counter drug labeled by Elevate Oral Care. The product's dosage form is paste, dentifrice and is administered via topical form.

    Is NDC 57511-0102 included in the NDC Directory?

    Yes, Fluorimax 5000 Sensitive with product code 57511-0102 is active and included in the NDC Directory. The product was first marketed by Elevate Oral Care on August 01, 2017.

    What is the 11-digit format for NDC 57511-0102-3?

    The 11-digit format is 57511010203. 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 5-4-1 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
    5-4-157511-0102-35-4-257511-0102-03