NDC 67659-501 Colgate Total Advanced Pro-shield Spearmint Surge
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 67659 - Team Technologies, Inc
- 67659-501 - Colgate Total Advanced Pro-shield Spearmint Surge
Product Characteristics
Product Packages
NDC Code 67659-501-30
Package Description: 1000 mL in 1 BOTTLE
Product Details
What is NDC 67659-501?
What are the uses for Colgate Total Advanced Pro-shield Spearmint Surge?
Which are Colgate Total Advanced Pro-shield Spearmint Surge UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- CETYLPYRIDINIUM (UNII: CUB7JI0JV3) (Active Moiety)
Which are Colgate Total Advanced Pro-shield Spearmint Surge 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:
- WATER (UNII: 059QF0KO0R)
- GLYCERIN (UNII: PDC6A3C0OX)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- SORBITOL (UNII: 506T60A25R)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- LEVOMENTHOL (UNII: BZ1R15MTK7)
- ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- FD&C GREEN NO. 3 (UNII: 3P3ONR6O1S)
- FD&C YELLOW NO. 6 (UNII: H77VEI93A8)
What is the NDC to RxNorm Crosswalk for Colgate Total Advanced Pro-shield Spearmint Surge?
- RxCUI: 1599135 - cetylpyridinium chloride 0.075 % Mouthwash
- RxCUI: 1599135 - cetylpyridinium chloride 0.75 MG/ML Mouthwash
- RxCUI: 1599137 - Colgate Total Advanced Pro-Shield 0.075 % Mouthwash
- RxCUI: 1599137 - cetylpyridinium chloride 0.75 MG/ML Mouthwash [Colgate Total Mouthwash]
- RxCUI: 1599137 - Colgate Total 0.75 MG/ML Mouthwash
* 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".