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  5. NDC Package Code: 72326-8001-1 Mintblast

NDC Package 72326-8001-1 Mintblast

Sodium Fluoride Paste 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:
72326-8001-1
Package Description:
28 g in 1 TUBE
Product Code:
72326-8001
Proprietary Name:
Mintblast
Non-Proprietary Name:
Sodium Fluoride
Substance Name:
Sodium Fluoride
Usage Information:
Adults and children 2 years of age  and  older: Brush teeth thoroughly, preferably after each  meal or at least twice a day,  or use as directed by a dentist or a physician.Children  2 to  6  years: Use only a  pea sized amount and supervise child's brushing and rinsing  (to minimize swallowing) .Children under 2 year : Ask a dentist or physician .
11-Digit NDC Billing Format:
72326800101
NDC to RxNorm Crosswalk:
  • RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
  • RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) Toothpaste
    • Product Type:
    Human Otc Drug
    Labeler Name:
    Young Ps Acquisition, Llc
    Dosage Form:
    Paste - A semisolid3 dosage form, containing a large proportion (20 – 50%) of solids finely dispersed in a fatty vehicle. This dosage form is generally for external application to the skin or mucous membranes.
    Administration Route(s):
  • Dental - Administration to a tooth or teeth.
    • Active Ingredient(s):
  • SODIUM FLUORIDE 2.43 mg/g
    • Sample Package:
    No
    FDA Application Number:
    part356
    Marketing Category:
    OTC MONOGRAPH NOT FINAL - A product marketed pursuant to an Over-the-Counter (OTC) Drug Monograph that is not final.
    Start Marketing Date:
    05-26-2018
    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 72326-8001-1?

    The NDC Packaged Code 72326-8001-1 is assigned to a package of 28 g in 1 tube of Mintblast, a human over the counter drug labeled by Young Ps Acquisition, Llc. The product's dosage form is paste and is administered via dental form.

    Is NDC 72326-8001 included in the NDC Directory?

    Yes, Mintblast with product code 72326-8001 is active and included in the NDC Directory. The product was first marketed by Young Ps Acquisition, Llc on May 26, 2018 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 72326-8001-1?

    The 11-digit format is 72326800101. 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
    5-4-172326-8001-15-4-272326-8001-01