NDC 36987-2297 Canary Grass
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
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Product Details
What is NDC 36987-2297?
What are the uses for Canary Grass?
Which are Canary Grass UNII Codes?
The UNII codes for the active ingredients in this product are:
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (Active Moiety)
- POA ANNUA POLLEN (UNII: 7U437HHU5C)
- POA ANNUA POLLEN (UNII: 7U437HHU5C) (Active Moiety)
- POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5)
- POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5) (Active Moiety)
- BROMUS INERMIS POLLEN (UNII: 766QT72BK6)
- BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (Active Moiety)
- PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9)
- PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9) (Active Moiety)
Which are Canary Grass 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:
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
- PHENOL (UNII: 339NCG44TV)
What is the NDC to RxNorm Crosswalk for Canary Grass?
- RxCUI: 1013966 - canary grass pollen extract 20,000 UNT/mL Injectable Solution
- RxCUI: 1013966 - canary grass pollen extract 20000 UNT/ML Injectable Solution
- RxCUI: 1013966 - Phalaris arundinacea pollen extract 20,000 UNT/ML Injectable Solution
- RxCUI: 1014347 - Italian rye grass pollen extract 20,000 UNT/mL Injectable Solution
- RxCUI: 1014347 - Italian rye grass pollen extract 20000 UNT/ML Injectable Solution
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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".