NDC 53247-200 Maximum Security Anticavity
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 53247 - Bob Barker Company, Inc.
- 53247-200 - Maximum Security Anticavity
Product Packages
NDC Code 53247-200-13
Package Description: 130 g in 1 TUBE
NDC Code 53247-200-42
Package Description: 4.25 g in 1 PACKET
Product Details
What is NDC 53247-200?
What are the uses for Maximum Security Anticavity?
Which are Maximum Security Anticavity 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 Maximum Security Anticavity 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)
- SORBITOL (UNII: 506T60A25R)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- SODIUM HYDROXIDE (UNII: 55X04QC32I)
- POLYOXYL 40 HYDROGENATED CASTOR OIL (UNII: 7YC686GQ8F)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- METHYL SALICYLATE (UNII: LAV5U5022Y)
What is the NDC to RxNorm Crosswalk for Maximum Security Anticavity?
- RxCUI: 245598 - sodium fluoride 0.22 % Toothpaste
- RxCUI: 245598 - sodium fluoride 0.0022 MG/MG Toothpaste
- RxCUI: 245598 - sodium fluoride 0.22 % (fluoride 0.1 % ) 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".