NDC 67659-330 Colgate Optic White Sparkling Mint Flavor
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67659 - Team Technologies, Inc
- 67659-330 - Colgate Optic White Sparkling Mint Flavor
Product Characteristics
Product Packages
NDC Code 67659-330-04
Package Description: 178 g in 1 TUBE
Product Details
What is NDC 67659-330?
What are the uses for Colgate Optic White Sparkling Mint Flavor?
Which are Colgate Optic White Sparkling Mint Flavor UNII Codes?
The UNII codes for the active ingredients in this product are:
- SODIUM MONOFLUOROPHOSPHATE (UNII: C810JCZ56Q)
- FLUORIDE ION (UNII: Q80VPU408O) (Active Moiety)
Which are Colgate Optic White Sparkling Mint Flavor 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:
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- CALCIUM PYROPHOSPHATE (UNII: X69NU20D19)
- GLYCERIN (UNII: PDC6A3C0OX)
- PEG/PPG-116/66 COPOLYMER (UNII: JP0CK963E0)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- POVIDONE K15 (UNII: E54VE15114)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- HYDROGEN PEROXIDE (UNII: BBX060AN9V)
- SODIUM ACID PYROPHOSPHATE (UNII: H5WVD9LZUD)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- BUTYLATED HYDROXYTOLUENE (UNII: 1P9D0Z171K)
What is the NDC to RxNorm Crosswalk for Colgate Optic White Sparkling Mint Flavor?
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.0076 MG/MG Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.12 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.13 % )Toothpaste
- RxCUI: 545626 - sodium monofluorophosphate 0.76 % (fluoride ion 0.14 % )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".