NDC 65954-022 Colgate Luminous Crystal Fluoride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65954 - Mission Hills S.a. De C.v.
- 65954-022 - Colgate Luminous Crystal Fluoride
Product Characteristics
Product Packages
NDC Code 65954-022-64
Package Description: 1 TUBE in 1 CARTON / 181 g in 1 TUBE
NDC Code 65954-022-69
Package Description: 1 TUBE in 1 CARTON / 113 g in 1 TUBE
Product Details
What is NDC 65954-022?
What are the uses for Colgate Luminous Crystal Fluoride?
Which are Colgate Luminous Crystal Fluoride 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 Colgate Luminous Crystal Fluoride 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)
- HYDRATED SILICA (UNII: Y6O7T4G8P9)
- POLYETHYLENE GLYCOL 600 (UNII: NL4J9F21N9)
- CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM PYROPHOSPHATE (UNII: O352864B8Z)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- MICA (UNII: V8A1AW0880)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- FD&C BLUE NO. 1 (UNII: H3R47K3TBD)
What is the NDC to RxNorm Crosswalk for Colgate Luminous Crystal Fluoride?
- RxCUI: 416783 - sodium fluoride 0.24 % Toothpaste
- RxCUI: 416783 - sodium fluoride 0.0024 MG/MG Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.13 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (fluoride ion 0.14 % ) Toothpaste
- RxCUI: 416783 - sodium fluoride 0.24 % (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".