1. Home
  2. Labeler Index
  3. Smiletwice, Inc.
  4. 72164-102
  5. NDC Package Code: 72164-102-23 Mini Duo

NDC Package 72164-102-23 Mini Duo

Potassium Nitrate,Sodium Fluoride Kit - 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:
72164-102-23
Package Description:
1 KIT in 1 KIT * 23 g in 1 TUBE (72164-001-02) * 23 g in 1 TUBE (72164-000-02)
Product Code:
72164-102
Proprietary Name:
Mini Duo
Non-Proprietary Name:
Potassium Nitrate, Sodium Fluoride
Usage Information:
Adults and children 12 years of age and older: Apply at least 1 inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly, for at least 1 minute twice a day (morning and night) or as recommended by a dentist or doctor. Make sure to brush all sensitive areas of the teeth. Minimize swallowing. Children under 12 years: consult a dentist or doctor.
11-Digit NDC Billing Format:
72164010223
NDC to RxNorm Crosswalk:
  • RxCUI: 1038929 - potassium nitrate 5 % / sodium fluoride 0.24 % Toothpaste
  • RxCUI: 1038929 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.0024 MG/MG Toothpaste
  • RxCUI: 1038929 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste
  • RxCUI: 1038929 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.0024 MG/MG Toothpaste
  • RxCUI: 1038929 - potassium nitrate 5 % / sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Smiletwice, Inc.
    Dosage Form:
    Kit - A packaged collection of related material.
    Sample Package:
    No
    FDA Application Number:
    part355B
    Marketing Category:
    OTC MONOGRAPH DRUG -
    Start Marketing Date:
    03-01-2020
    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 72164-102-23?

    The NDC Packaged Code 72164-102-23 is assigned to a package of 1 kit in 1 kit * 23 g in 1 tube (72164-001-02) * 23 g in 1 tube (72164-000-02) of Mini Duo, a human over the counter drug labeled by Smiletwice, Inc.. The product's dosage form is kit and is administered via form.

    Is NDC 72164-102 included in the NDC Directory?

    Yes, Mini Duo with product code 72164-102 is active and included in the NDC Directory. The product was first marketed by Smiletwice, Inc. on March 01, 2020 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 72164-102-23?

    The 11-digit format is 72164010223. 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
    5-3-272164-102-235-4-272164-0102-23