NDC 67659-082 Up And Up Anticavity Toothpaste Whitening
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67659 - Team Technologies, Inc
- 67659-082 - Up And Up Anticavity Toothpaste Whitening
Product Characteristics
Product Packages
NDC Code 67659-082-02
Package Description: 1 TUBE in 1 CARTON / 181.4 g in 1 TUBE (67659-082-01)
Product Details
What is NDC 67659-082?
What are the uses for Up And Up Anticavity Toothpaste Whitening?
Which are Up And Up Anticavity Toothpaste Whitening UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM FLUORIDE (UNII: 8ZYQ1474W7)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Up And Up Anticavity Toothpaste 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)
- WATER (UNII: 059QF0KO0R)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SODIUM PHOSPHATE (UNII: SE337SVY37)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Up And Up Anticavity Toothpaste Whitening?
- RxCUI: 891775 - sodium fluoride 0.243 % Toothpaste
- RxCUI: 891775 - sodium fluoride 0.00243 MG/MG Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 891775 - sodium fluoride 0.243 % (fluoride ion 0.15 % ) 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".