NDC 67225-0009 2080 Dentistry Night Fresh
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 67225-0009?
What are the uses for 2080 Dentistry Night Fresh?
Which are 2080 Dentistry Night Fresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4) (Active Moiety)
Which are 2080 Dentistry Night Fresh 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:
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- ZINC CITRATE TRIHYDRATE (UNII: GNM26GAX7R)
- GLYCYRRHIZINATE DIPOTASSIUM (UNII: CA2Y0FE3FX)
- SORBITOL (UNII: 506T60A25R)
- GLYCERIN (UNII: PDC6A3C0OX)
- POLYETHYLENE GLYCOL 1500 (UNII: 1212Z7S33A)
- SODIUM ALGINATE (UNII: C269C4G2ZQ)
- SODIUM CITRATE (UNII: 1Q73Q2JULR)
- SACCHARIN SODIUM (UNII: SB8ZUX40TY)
- COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)
- SODIUM LAURYL SULFATE (UNII: 368GB5141J)
- SODIUM METHYL COCOYL TAURATE (UNII: JVL98CG53G)
- TITANIUM DIOXIDE (UNII: 15FIX9V2JP)
- THYMUS VULGARIS LEAF (UNII: GRX3499643)
- CYMBOPOGON CITRATUS WHOLE (UNII: 6AE8LT94NG)
- PELARGONIUM GRAVEOLENS WHOLE (UNII: 0E553RP62F)
- CINNAMON BARK OIL (UNII: XE54U569EC)
- FENNEL SEED (UNII: G3QC02NIE6)
- ROSEMARY (UNII: IJ67X351P9)
- CLOVE (UNII: K48IKT5321)
- WATER (UNII: 059QF0KO0R)
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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".