NDC 0363-0631 Walgreens Maximum Strength Sensitive Fluoride

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:
0363-0631
Proprietary Name:
Walgreens Maximum Strength Sensitive Fluoride
Product Type: [3]
INACTIVATED PRODUCT and EXCLUDED the from NDC Directory
Labeler Name: [5]
Walgreens
Labeler Code:
0363
Start Marketing Date: [9]
06-06-2006
Listing Expiration Date: [11]
12-31-2017
Exclude Flag: [12]
I
Code Structure:
Code Navigator:

Product Characteristics

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

Product Packages

NDC Code 0363-0631-09

Package Description: 113 g in 1 TUBE

Product Details

What is NDC 0363-0631?

The NDC code 0363-0631 is assigned by the FDA to the product Walgreens Maximum Strength Sensitive Fluoride which is product labeled by Walgreens. The product's dosage form is . The product is distributed in a single package with assigned NDC code 0363-0631-09 113 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 Walgreens Maximum Strength Sensitive Fluoride?

Adults and children     Brush teeth for at least one minute, preferably after 12 years and older      each meal, or at least twice a day or as directed by                                   your dentist. Be sure to brush sensitive areas.Children under           Consult a dentist or doctor 12 years of age             Other information        Store in a cool, dry place.

Which are Walgreens Maximum Strength Sensitive Fluoride UNII Codes?

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

Which are Walgreens Maximum Strength Sensitive Fluoride 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 Walgreens Maximum Strength Sensitive Fluoride?

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

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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".