NDC 49288-0807 Treatment Set Ts340074
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 49288 - Antigen Laboratories, Inc.
- 49288-0807 - Treatment Set Ts340074
Product Packages
NDC Code 49288-0807-3
Package Description: 10 mL in 1 VIAL, MULTI-DOSE
Product Details
What is NDC 49288-0807?
What are the uses for Treatment Set Ts340074?
Which are Treatment Set Ts340074 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)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3)
- AMBROSIA ARTEMISIIFOLIA POLLEN (UNII: K20Y81ACO3) (Active Moiety)
- CARYA ALBA POLLEN (UNII: G2A764T54B)
- CARYA TOMENTOSA POLLEN (UNII: G2A764T54B) (Active Moiety)
- DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q)
- DERMATOPHAGOIDES FARINAE (UNII: PR9U2YPF3Q) (Active Moiety)
- DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K)
- DERMATOPHAGOIDES PTERONYSSINUS (UNII: 57L1Z5378K) (Active Moiety)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR)
- CANIS LUPUS FAMILIARIS HAIR (UNII: 05S7L91ZTR) (Active Moiety)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR)
- JUGLANS NIGRA POLLEN (UNII: 1BV28146ZR) (Active Moiety)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD)
- ULMUS AMERICANA POLLEN (UNII: 89BAT511BD) (Active Moiety)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG)
- PHLEUM PRATENSE POLLEN (UNII: 65M88RW2EG) (Active Moiety)
- IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22)
- IVA ANNUA VAR. ANNUA POLLEN (UNII: Y2U5S5PF22) (Active Moiety)
- CARYA TOMENTOSA POLLEN (UNII: G2A764T54B)
Which are Treatment Set Ts340074 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".