NDC 49288-0239 Mixture Of Standardized And Non-standardized Southern Grasses
View Dosage, Usage, Ingredients, Routes, UNII
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What is NDC 49288-0239?
What are the uses for Mixture Of Standardized And Non-standardized Southern Grasses?
Which are Mixture Of Standardized And Non-standardized Southern Grasses UNII Codes?
The UNII codes for the active ingredients in this product are:
- CYNODON DACTYLON POLLEN (UNII: 175F461W10)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
- DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P)
- DACTYLIS GLOMERATA POLLEN (UNII: 83N78IDA7P) (Active Moiety)
- AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA)
- AGROSTIS GIGANTEA POLLEN (UNII: HU8V6E7HOA) (Active Moiety)
- LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0)
- LOLIUM PERENNE POLLEN (UNII: 4T81LB52R0) (Active Moiety)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y)
- ANTHOXANTHUM ODORATUM POLLEN (UNII: 2KIK19R45Y) (Active Moiety)
- POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5)
- POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5) (Active Moiety)
- TYPHA LATIFOLIA POLLEN (UNII: 341PDX5PLM)
- TYPHA LATIFOLIA POLLEN (UNII: 341PDX5PLM) (Active Moiety)
- BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046)
- BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046) (Active Moiety)
- ZEA MAYS POLLEN (UNII: 74PD8J616H)
- ZEA MAYS POLLEN (UNII: 74PD8J616H) (Active Moiety)
- SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O)
- SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O) (Active Moiety)
- TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D)
- TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- ELYMUS REPENS POLLEN (UNII: ON2T85TA2O)
- ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (Active Moiety)
- PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9)
- PHALARIS ARUNDINACEA POLLEN (UNII: FAY1Y90VJ9) (Active Moiety)
- BROMUS INERMIS POLLEN (UNII: 766QT72BK6)
- BROMUS INERMIS POLLEN (UNII: 766QT72BK6) (Active Moiety)
- SORGHUM BICOLOR SSP. DRUMMONDII POLLEN (UNII: B43R30VP73)
- SORGHUM BICOLOR SSP. DRUMMONDII POLLEN (UNII: B43R30VP73) (Active Moiety)
- ARRHENATHERUM ELATIUS POLLEN (UNII: B55BD1QM4Q)
- ARRHENATHERUM ELATIUS POLLEN (UNII: B55BD1QM4Q) (Active Moiety)
- HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01)
- HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (Active Moiety)
- PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O)
- PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O) (Active Moiety)
Which are Mixture Of Standardized And Non-standardized Southern Grasses 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:
- GLYCERIN (UNII: PDC6A3C0OX)
- WATER (UNII: 059QF0KO0R)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
What is the NDC to RxNorm Crosswalk for Mixture Of Standardized And Non-standardized Southern Grasses?
- RxCUI: 851873 - redtop grass pollen extract 100000 BAU/ML Injectable Solution
- RxCUI: 851873 - Agrostis gigantea pollen extract 100,000 BAU/ML Injectable Solution
- RxCUI: 852157 - Timothy grass pollen extract 100000 BAU/mL Injectable Solution
- RxCUI: 852157 - Timothy grass pollen extract 100000 BAU/ML Injectable Solution
- RxCUI: 852157 - Phleum pratense grass pollen extract 100,000 BAU/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".