NDC 49288-0802 Treatment Set Ts339754
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49288 - Antigen Laboratories, Inc.
- 49288-0802 - Treatment Set Ts339754
Product Packages
NDC Code 49288-0802-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 49288-0802?
What are the uses for Treatment Set Ts339754?
Which are Treatment Set Ts339754 UNII Codes?
The UNII codes for the active ingredients in this product are:
- FELIS CATUS HAIR (UNII: 1564HD0N96)
- FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10)
- CYNODON DACTYLON POLLEN (UNII: 175F461W10) (Active Moiety)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP)
- SORGHUM HALEPENSE POLLEN (UNII: 577VA5B4HP) (Active Moiety)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T)
- POA PRATENSIS POLLEN (UNII: SCB8J7LS3T) (Active Moiety)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK)
- PASPALUM NOTATUM POLLEN (UNII: V003SHB7VK) (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)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI)
- PLANTAGO LANCEOLATA POLLEN (UNII: DO87T1U2CI) (Active Moiety)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1)
- FESTUCA PRATENSIS POLLEN (UNII: A0WFQ8P6N1) (Active Moiety)
- CARYA ALBA POLLEN (UNII: G2A764T54B)
- CARYA ALBA POLLEN (UNII: G2A764T54B) (Active Moiety)
Which are Treatment Set Ts339754 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)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- GLYCERIN (UNII: PDC6A3C0OX)
- PHENOL (UNII: 339NCG44TV)
* 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".