NDC 49288-0276 Johnson Grass Pollen
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49288 - Antigen Laboratories, Inc.
- 49288-0276 - Johnson Grass Pollen
Product Packages
NDC Code 49288-0276-1
Package Description: 2 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0276-2
Package Description: 5 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0276-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0276-4
Package Description: 30 mL in 1 VIAL, MULTI-DOSE
NDC Code 49288-0276-5
Package Description: 50 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 49288-0276?
What are the uses for Johnson Grass Pollen?
Which are Johnson Grass Pollen UNII Codes?
The UNII codes for the active ingredients in this product are:
- BETA VULGARIS POLLEN (UNII: W7NU4B5CIY)
- BETA VULGARIS POLLEN (UNII: W7NU4B5CIY) (Active Moiety)
- ZEA MAYS POLLEN (UNII: 74PD8J616H)
- ZEA MAYS POLLEN (UNII: 74PD8J616H) (Active Moiety)
- MELILOTUS ALBUS POLLEN (UNII: 9L67M8B78R)
- MELILOTUS ALBUS POLLEN (UNII: 9L67M8B78R) (Active Moiety)
- POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5)
- POA COMPRESSA POLLEN (UNII: 50HCQ1NYV5) (Active Moiety)
- POA ANNUA POLLEN (UNII: 7U437HHU5C)
- POA ANNUA POLLEN (UNII: 7U437HHU5C) (Active Moiety)
- BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046)
- BROMUS SECALINUS POLLEN (UNII: Q4T1SJ3046) (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)
- TYPHA LATIFOLIA POLLEN (UNII: 341PDX5PLM)
- TYPHA LATIFOLIA POLLEN (UNII: 341PDX5PLM) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- ARRHENATHERUM ELATIUS POLLEN (UNII: B55BD1QM4Q)
- ARRHENATHERUM ELATIUS POLLEN (UNII: B55BD1QM4Q) (Active Moiety)
- AVENA SATIVA POLLEN (UNII: A7IKY24TR7)
- AVENA SATIVA POLLEN (UNII: A7IKY24TR7) (Active Moiety)
- ELYMUS REPENS POLLEN (UNII: ON2T85TA2O)
- ELYMUS REPENS POLLEN (UNII: ON2T85TA2O) (Active Moiety)
- SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O)
- SECALE CEREALE POLLEN (UNII: I6KAZ8AO1O) (Active Moiety)
- SORGHUM BICOLOR SSP. DRUMMONDII POLLEN (UNII: B43R30VP73)
- SORGHUM BICOLOR SSP. DRUMMONDII POLLEN (UNII: B43R30VP73) (Active Moiety)
- DISTICHLIS SPICATA POLLEN (UNII: GOA51670YV)
- DISTICHLIS SPICATA POLLEN (UNII: GOA51670YV) (Active Moiety)
- HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01)
- HOLCUS LANATUS POLLEN (UNII: 70O1TP6H01) (Active Moiety)
- TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D)
- TRITICUM AESTIVUM POLLEN (UNII: F1KAH8374D) (Active Moiety)
- PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O)
- PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O) (Active Moiety)
- MELILOTUS OFFICINALIS POLLEN (UNII: UVC3Z60VTX)
- MELILOTUS OFFICINALIS POLLEN (UNII: UVC3Z60VTX) (Active Moiety)
Which are Johnson Grass Pollen 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)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- WATER (UNII: 059QF0KO0R)
What is the NDC to RxNorm Crosswalk for Johnson Grass Pollen?
- RxCUI: 1006509 - tall oat grass pollen extract 50 MG/ML Injectable Solution
- RxCUI: 1006509 - Arrhenatherum elatius pollen extract 0.05 GM/ML Injectable Solution
- RxCUI: 1006509 - Arrhenatherum elatius pollen extract 1 GM per 20 ML Injectable Solution
- RxCUI: 1006509 - Arrhenatherum elatius pollen extract 50 MG/ML Injectable Solution
- RxCUI: 1014734 - Canadian bluegrass pollen extract 50 MG/mL Injectable Solution
* Please review the disclaimer below.
[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".