NDC 49288-0943 Treatment Set Ts350663
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49288-0943?
What are the uses for Treatment Set Ts350663?
Which are Treatment Set Ts350663 UNII Codes?
The UNII codes for the active ingredients in this product are:
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
- PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O)
- PASCOPYRUM SMITHII POLLEN (UNII: 6AU0ZD8T1O) (Active Moiety)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
- PERIPLANETA AMERICANA (UNII: 2RQ1L9N089)
- PERIPLANETA AMERICANA (UNII: 2RQ1L9N089) (Active Moiety)
- DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K)
- DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Active Moiety)
- COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W)
- COCHLIOBOLUS SATIVUS (UNII: 3LN5B70U4W) (Active Moiety)
- BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U)
- BETULA POPULIFOLIA POLLEN (UNII: 23H70FYJ5U) (Active Moiety)
- POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP)
- POPULUS DELTOIDES POLLEN (UNII: 476DVV63WP) (Active Moiety)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
- POPULUS NIGRA POLLEN (UNII: 0MGE63QPFJ)
- POPULUS NIGRA POLLEN (UNII: 0MGE63QPFJ) (Active Moiety)
- POPULUS ALBA POLLEN (UNII: VU8C8SB23P)
- POPULUS ALBA POLLEN (UNII: VU8C8SB23P) (Active Moiety)
Which are Treatment Set Ts350663 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:
- WATER (UNII: 059QF0KO0R)
- PHENOL (UNII: 339NCG44TV)
- GLYCERIN (UNII: PDC6A3C0OX)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
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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".