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  4. NDC Product Code: 72326-8011 Mintblast

NDC 72326-8011 Mintblast

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72326-8011?
  5. Mintblast Uses
  6. Active Ingredients UNII Codes
  7. Inactive Ingredients UNII Codes
  8. NDC to RxNorm Crosswalk

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
72326-8011
Proprietary Name:
Mintblast
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Young Ps Acquisition, Llc
Labeler Code:
72326
Product Label ID:
7b0b1034-c246-4518-821a-181c78ad6d4e
Start Marketing Date: [9]
05-26-2018
Listing Expiration Date: [11]
12-31-2019
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Flavor(s):
MINT (C73404 - MINT)

Product Packages

NDC Code 72326-8011-1

Package Description: 28 g in 1 TUBE

Product Details

What is NDC 72326-8011?

The NDC code 72326-8011 is assigned by the FDA to the product Mintblast which is product labeled by Young Ps Acquisition, Llc. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72326-8011-1 28 g in 1 tube . This page includes all the important details about this product, including active and inactive ingredients, pharmagologic classes, product uses and characteristics, UNII information and RxNorm crosswalk.

What are the uses for Mintblast?

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 .

Which are Mintblast UNII Codes?

The UNII codes for the active ingredients in this product are:

Which are Mintblast Inactive Ingredients UNII Codes?

The inactive ingredients are all the component of a medicinal product OTHER than the active ingredient(s). The acronym "UNII" stands for “Unique Ingredient Identifier” and is used to identify each inactive ingredient present in a product. The UNII codes for the inactive ingredients in this product are:

What is the NDC to RxNorm Crosswalk for Mintblast?

RxNorm is a normalized naming system for generic and branded drugs that assigns unique concept identifier(s) known as RxCUIs to NDC products.The NDC to RxNorm Crosswalk for this produdct indicates multiple concept unique identifiers (RXCUIs) are associated with this product:
  • 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

* Please review the disclaimer below.

Product Footnotes

[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.

[9] What is the Start Marketing Date? - This is the date that the labeler indicates was the start of its marketing of the drug product.

[11] What is the Listing Expiration Date? - This is the date when the listing record will expire if not updated or certified by the product labeler.

[12] What is the NDC Exclude Flag? - This field indicates whether the product has been removed/excluded from the NDC Directory for failure to respond to FDA"s requests for correction to deficient or non-compliant submissions ("Y"), or because the listing certification is expired ("E"), or because the listing data was inactivated by FDA ("I"). Values = "Y", "N", "E", or "I".