NDC 67659-160 Dentemp Canker Sore Single Dose
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Product Details
What is NDC 67659-160?
What are the uses for Dentemp Canker Sore Single Dose?
Which are Dentemp Canker Sore Single Dose UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Dentemp Canker Sore Single Dose 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:
- POVIDONE K90 (UNII: RDH86HJV5Z)
- ANNATTO (UNII: 6PQP1V1B6O)
- CARBOMER HOMOPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: F68VH75CJC)
- MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
- CITRUS LIMON FRUIT OIL (UNII: 0HNC1J1YED)
- HYDROXYPROPYL CELLULOSE, UNSPECIFIED (UNII: 9XZ8H6N6OH)
- POVIDONE K30 (UNII: U725QWY32X)
- XYLITOL (UNII: VCQ006KQ1E)
- SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
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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".