NDC 82340-002 Kofix Cherry And Blackberry
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Product Characteristics
BLACKBERRY (C73366)
Code Structure Chart
Product Details
What is NDC 82340-002?
What are the uses for Kofix Cherry And Blackberry?
Which are Kofix Cherry And Blackberry UNII Codes?
The UNII codes for the active ingredients in this product are:
- MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A)
- MENTHOL (UNII: L7T10EIP3A) (Active Moiety)
Which are Kofix Cherry And Blackberry 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:
- ANETHOLE (UNII: Q3JEK5DO4K)
- BLACK CURRANT JUICE (UNII: 9L8NK01P32)
- CARMINIC ACID (UNII: CID8Z8N95N)
- CITRIC ACID MONOHYDRATE (UNII: 2968PHW8QP)
- CLOVE OIL (UNII: 578389D6D0)
- STARCH, CORN (UNII: O8232NY3SJ)
- EUCALYPTUS OIL (UNII: 2R04ONI662)
- ACACIA (UNII: 5C5403N26O)
- SUCROSE (UNII: C151H8M554)
What is the NDC to RxNorm Crosswalk for Kofix Cherry And Blackberry?
- RxCUI: 1039799 - menthol 8 MG Oral Lozenge
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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".