NDC 51009-213 Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners

View Dosage, Usage, Ingredients, Routes, UNII

Product Information

This product is EXCLUDED from the official NDC directory because the listing data was inactivated by the FDA.
NDC Product Code:
51009-213
Proprietary Name:
Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Tom's Of Maine, Inc.
Labeler Code:
51009
Start Marketing Date: [9]
03-01-2015
Listing Expiration Date: [11]
12-31-2022
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

Color(s):
WHITE (C48325)
Flavor(s):
MINT (C73404 - SOOTHING MINT)

Product Packages

NDC Code 51009-213-40

Package Description: 1 TUBE in 1 CARTON / 113 g in 1 TUBE

Product Details

What is NDC 51009-213?

The NDC code 51009-213 is assigned by the FDA to the product Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners which is product labeled by Tom's Of Maine, Inc.. The product's dosage form is . The product is distributed in a single package with assigned NDC code 51009-213-40 1 tube in 1 carton / 113 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 Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners?

Adults and children 12 years of age and older apply at least a 1-inch strip of the product onto a soft bristle toothbrush. Brush teeth thoroughly at least 1 minute twice a day (morning and evening) or as recommended by a dentist or physician. Make sure to brush all sensitive areas of the teeth.children under 12 years of age: consult a dentist or physician

Which are Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners UNII Codes?

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

Which are Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners 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 Toms Natural Maximum Strength Sensitive Soothing Mint Clinically Proven To Reduce Painful Sensitivity / No Artificial Dyes Or Sweeteners?

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: 1038800 - potassium nitrate 5 % / sodium fluoride 0.243 % (fluoride ion 0.14 % - 0.15 % ) Toothpaste
  • RxCUI: 1038800 - potassium nitrate 0.05 MG/MG / sodium fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 1038800 - K+ nitrate 0.05 MG/MG / Sodium Fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 1038800 - Pot nitrate 0.05 MG/MG / Sodium Fluoride 0.00243 MG/MG Toothpaste
  • RxCUI: 1038800 - potassium nitrate 5 % / 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".