NDC 51009-197 Sensitive Fluoride-free - Wintermint
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 51009 - Tom's Of Maine, Inc.
- 51009-197 - Sensitive
Product Characteristics
Product Packages
NDC Code 51009-197-04
Package Description: 1 TUBE in 1 CARTON / 113 g in 1 TUBE
Product Details
What is NDC 51009-197?
What are the uses for Sensitive Fluoride-free - Wintermint?
Which are Sensitive Fluoride-free - Wintermint UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- POTASSIUM CATION (UNII: 295O53K152) (Active Moiety)
Which are Sensitive Fluoride-free - Wintermint 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:
- SORBITOL (UNII: 506T60A25R)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- XYLITOL (UNII: VCQ006KQ1E)
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- XANTHAN GUM (UNII: TTV12P4NEE)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- MENTHOL (UNII: L7T10EIP3A)
- GLYCYRRHIZIN (UNII: 6FO62043WK)
What is the NDC to RxNorm Crosswalk for Sensitive Fluoride-free - Wintermint?
- RxCUI: 312544 - potassium nitrate 5 % Toothpaste
- RxCUI: 312544 - potassium nitrate 0.05 MG/MG Toothpaste
- RxCUI: 312544 - K+ nitrate 0.05 MG/MG Toothpaste
- RxCUI: 312544 - Pot nitrate 0.05 MG/MG Toothpaste
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[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".