NDC 29494-1104 Vividsensiguard
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 29494 - Pearson Dental Supply Co.
- 29494-1104 - Vividsensiguard
Product Characteristics
BUBBLE GUM (C73368)
Product Packages
NDC Code 29494-1104-2
Package Description: 56.7 g in 1 TUBE
Product Details
What is NDC 29494-1104?
What are the uses for Vividsensiguard?
Which are Vividsensiguard 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 Vividsensiguard 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:
- XYLITOL (UNII: VCQ006KQ1E)
- CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)
- TRIBASIC CALCIUM PHOSPHATE (UNII: 91D9GV0Z28)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SODIUM PHOSPHATE, DIBASIC (UNII: GR686LBA74)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BENZOATE (UNII: OJ245FE5EU)
- SUCRALOSE (UNII: 96K6UQ3ZD4)
- SODIUM PHOSPHATE, MONOBASIC (UNII: 3980JIH2SW)
- WATER (UNII: 059QF0KO0R)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
What is the NDC to RxNorm Crosswalk for Vividsensiguard?
- RxCUI: 1486566 - sodium fluoride 1.1 % Oral Gel
- RxCUI: 1486566 - sodium fluoride 0.011 MG/MG Oral Gel
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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".