NDC 86157-0014 Denti Whoo Blue Tabletgargle
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 86157 - Sun Life Science Co Ltd
- 86157-0014 - Denti Whoo Blue Tabletgargle
Product Characteristics
Product Packages
NDC Code 86157-0014-1
Package Description: 8 TABLET in 1 PACKAGE
Product Details
What is NDC 86157-0014?
What are the uses for Denti Whoo Blue Tabletgargle?
Which are Denti Whoo Blue Tabletgargle 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 Denti Whoo Blue Tabletgargle 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:
- TARTARIC ACID (UNII: W4888I119H)
- MALTITOL (UNII: D65DG142WK)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
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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".