NDC 0363-0632 Walgreen Sensitive Extra Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 0363 - Walgreen
- 0363-0632 - Walgreen Sensitive Extra Whitening
Product Characteristics
Product Packages
NDC Code 0363-0632-72
Package Description: 113 g in 1 TUBE
Product Details
What is NDC 0363-0632?
What are the uses for Walgreen Sensitive Extra Whitening?
Which are Walgreen Sensitive Extra Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- POTASSIUM NITRATE (UNII: RU45X2JN0Z)
- NITRATE ION (UNII: T93E9Y2844) (Active Moiety)
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Walgreen Sensitive Extra Whitening 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)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- WATER (UNII: 059QF0KO0R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
What is the NDC to RxNorm Crosswalk for Walgreen Sensitive Extra Whitening?
- 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.
[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".