NDC 51414-500 Mouth Fresh
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 51414-500?
What are the uses for Mouth Fresh?
Which are Mouth Fresh UNII Codes?
The UNII codes for the active ingredients in this product are:
- CETYLPYRIDINIUM CHLORIDE (UNII: D9OM4SK49P)
- CETYLPYRIDINIUM (UNII: CUB7JI0JV3) (Active Moiety)
Which are Mouth 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:
- WATER (UNII: 059QF0KO0R)
- PROPYLENE GLYCOL (UNII: 6DC9Q167V3)
- DISODIUM EDTA-COPPER (UNII: 6V475AX06U)
- CHLOROMETHYL METHYL ETHER (UNII: 334G5B96VG)
- POTASSIUM SORBATE (UNII: 1VPU26JZZ4)
- QUATERNIUM-15 (UNII: E40U03LEM0)
- DISODIUM COCOAMPHODIACETATE (UNII: 18L9G3U51M)
- ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
- POLYSORBATE 20 (UNII: 7T1F30V5YH)
- CITRIC ACID ACETATE (UNII: DSO12WL7AU)
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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".