NDC 65044-4351 Animal Allergens, Feather Mix
View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 65044 - Jubilant Hollisterstier Llc
- 65044-4351 - Animal Allergens, Feather Mix
Product Packages
NDC Code 65044-4351-5
Package Description: 5 mL in 1 VIAL
Product Details
What is NDC 65044-4351?
What are the uses for Animal Allergens, Feather Mix?
Which are Animal Allergens, Feather Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- EQUUS CABALLUS HAIR (UNII: 4F35XG0149)
- EQUUS CABALLUS HAIR (UNII: 4F35XG0149) (Active Moiety)
- EQUUS CABALLUS DANDER (UNII: J81SZ18495)
- EQUUS CABALLUS DANDER (UNII: J81SZ18495) (Active Moiety)
- BOS TAURUS HAIR (UNII: TOQ97Z8644)
- BOS TAURUS HAIR (UNII: TOQ97Z8644) (Active Moiety)
- BOS TAURUS DANDER (UNII: C8VYS726O8)
- BOS TAURUS DANDER (UNII: C8VYS726O8) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- ANSER ANSER FEATHER (UNII: 15XI414745)
- ANSER ANSER FEATHER (UNII: 15XI414745) (Active Moiety)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
Which are Animal Allergens, Feather Mix 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:
- PHENOL (UNII: 339NCG44TV)
- SODIUM CHLORIDE (UNII: 451W47IQ8X)
- SODIUM BICARBONATE (UNII: 8MDF5V39QO)
- GLYCERIN (UNII: PDC6A3C0OX)
What is the NDC to RxNorm Crosswalk for Animal Allergens, Feather Mix?
- RxCUI: 1006369 - Canada goldenrod pollen extract 500 UNT/ML Injectable Solution
- RxCUI: 1006369 - Solidago canadensis pollen extract 500 UNT/ML Injectable Solution
- RxCUI: 1087970 - Mucor racemosus allergenic extract 1000 UNT/mL Injectable Solution
- RxCUI: 1087970 - Mucor racemosus allergenic extract 1000 UNT/ML Injectable Solution
- RxCUI: 1087970 - Mucor racemosus extract 1000 UNT/ML Injectable Solution
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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".