NDC 50227-0541 Topical 60 Sec Sodium Fluoride Orange Cream
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
Code Structure Chart
Product Details
What is NDC 50227-0541?
What are the uses for Topical 60 Sec Sodium Fluoride Orange Cream?
Which are Topical 60 Sec Sodium Fluoride Orange Cream 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 Topical 60 Sec Sodium Fluoride Orange Cream 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:
- SACCHARIN SODIUM DIHYDRATE (UNII: SB8ZUX40TY)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)
- CETYL PHOSPHATE (UNII: VT07D6X67O)
- CETYL ALCOHOL (UNII: 936JST6JCN)
- OLETH-3 PHOSPHATE (UNII: 8Q0Z18J1VL)
- SODIUM PHOSPHATE, MONOBASIC, MONOHYDRATE (UNII: 593YOG76RN)
- APAFLURANE (UNII: R40P36GDK6)
- BENZALDEHYDE (UNII: TA269SD04T)
What is the NDC to RxNorm Crosswalk for Topical 60 Sec Sodium Fluoride Orange Cream?
- RxCUI: 248389 - sodium fluoride 2.72 % Oral Foam
- RxCUI: 248389 - sodium fluoride 27.2 MG/ML Oral Foam
- RxCUI: 248389 - sodium fluoride 2.72 % (fluoride ion 1.23 % ) Oral Foam
* 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".