NDC 49288-0784 Treatment Set Ts336924
View Dosage, Usage, Ingredients, Routes, UNII
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Product Details
What is NDC 49288-0784?
What are the uses for Treatment Set Ts336924?
Which are Treatment Set Ts336924 UNII Codes?
The UNII codes for the active ingredients in this product are:
- DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K)
- DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K) (Active Moiety)
- DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q)
- DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q) (Active Moiety)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG)
- PENICILLIUM CHRYSOGENUM VAR. CHRYSOGENUM (UNII: 3Y1PE1GCIG) (Active Moiety)
- CLADOSPORIUM HERBARUM (UNII: O64JF11198)
- CLADOSPORIUM HERBARUM (UNII: O64JF11198) (Active Moiety)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48)
- ASPERGILLUS FUMIGATUS (UNII: X88DF51T48) (Active Moiety)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H)
- ALTERNARIA ALTERNATA (UNII: 52B29REC7H) (Active Moiety)
- FELIS CATUS HAIR (UNII: 1564HD0N96)
- FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
- ACER NEGUNDO POLLEN (UNII: P6K070AR8V)
- ACER NEGUNDO POLLEN (UNII: P6K070AR8V) (Active Moiety)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q)
- FRAXINUS AMERICANA POLLEN (UNII: G684LX721Q) (Active Moiety)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK)
- QUERCUS ALBA POLLEN (UNII: Z4Y9ZSV4KK) (Active Moiety)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y)
- CARYA ILLINOINENSIS POLLEN (UNII: PYO4JR720Y) (Active Moiety)
- CARYA ALBA POLLEN (UNII: G2A764T54B)
- CARYA ALBA POLLEN (UNII: G2A764T54B) (Active Moiety)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- SALSOLA KALI POLLEN (UNII: 2MH135KC6G)
- SALSOLA KALI POLLEN (UNII: 2MH135KC6G) (Active Moiety)
Which are Treatment Set Ts336924 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)
- 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".