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  4. NDC Product Code: 72916-312 Schmidts Mint And Berry Kids Tooth And Mouth

NDC 72916-312 Schmidts Mint And Berry Kids Tooth And Mouth

View Dosage, Usage, Ingredients, Routes, UNII

Table of Contents

  1. Product Information
  2. Product Packages
  3. Product Characteristics
  4. What is NDC 72916-312?
  5. Schmidts Mint And Berry Kids Tooth And Mouth 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:
72916-312
Proprietary Name:
Schmidts Mint And Berry Kids Tooth And Mouth
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Schmidt's Naturals
Labeler Code:
72916
Product Label ID:
e663d84c-a4e9-4fb9-aa30-caf0bb1428db
Start Marketing Date: [9]
06-20-2019
Listing Expiration Date: [11]
12-31-2020
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404)
BERRY (C73365)

Product Packages

NDC Code 72916-312-05

Package Description: 1 TUBE in 1 CARTON / 133 g in 1 TUBE

Product Details

What is NDC 72916-312?

The NDC code 72916-312 is assigned by the FDA to the product Schmidts Mint And Berry Kids Tooth And Mouth which is product labeled by Schmidt's Naturals. The product's dosage form is . The product is distributed in a single package with assigned NDC code 72916-312-05 1 tube in 1 carton / 133 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 Schmidts Mint And Berry Kids Tooth And Mouth?

Adults and children 2 years of age and older:Brush teeth thoroughly, preferably after each meal or at least twice a day or as directed by a Dentist or Physician.Children 2 to 6 years of age:Instruct children under 6 years of age in good brushing and rinsing methods (to minimize swallowing). Supervise children as necessary until capable of using without supervision.Children under 2 years of age: Consult a Dentist or Physician.

Which are Schmidts Mint And Berry Kids Tooth And Mouth UNII Codes?

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

Which are Schmidts Mint And Berry Kids Tooth And Mouth 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 Schmidts Mint And Berry Kids Tooth And Mouth?

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: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
  • RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )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".