NDC 69638-068 Scotts Select Apf Foam Fluoride
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 69638 - Scotts Dental Supply Llc
- 69638-068 - Scotts Select Apf Foam Fluoride
Product Characteristics
Product Packages
NDC Code 69638-068-04
Package Description: 130 mL in 1 BOTTLE
Product Details
What is NDC 69638-068?
What are the uses for Scotts Select Apf Foam Fluoride?
Which are Scotts Select Apf Foam 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 Scotts Select Apf Foam 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:
- CASTOR OIL (UNII: D5340Y2I9G)
- DECYL GLUCOSIDE (UNII: Z17H97EA6Y)
- WATER (UNII: 059QF0KO0R)
- HYDROFLUORIC ACID (UNII: RGL5YE86CZ)
- PHOSPHORIC ACID (UNII: E4GA8884NN)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SODIUM LAURETH-3 SULFATE (UNII: BPV390UAP0)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- XYLITOL (UNII: VCQ006KQ1E)
- POLOXAMER 407 (UNII: TUF2IVW3M2)
- TROLAMINE (UNII: 9O3K93S3TK)
What is the NDC to RxNorm Crosswalk for Scotts Select Apf Foam Fluoride?
- RxCUI: 831719 - sodium fluoride 1.23 % Oral Foam
- RxCUI: 831719 - sodium fluoride 12.3 MG/ML Oral Foam
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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".