NDC 44911-0452 Animal Antigens
Canary Feathers,Cat Hair,Cattle Epithelia,Chicken Feathers,Dog Epithelia,Duck - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
Code Structure Chart
Product Details
What is NDC 44911-0452?
What are the uses for Animal Antigens?
What are Animal Antigens Active Ingredients?
- ANAS PLATYRHYNCHOS FEATHER 9 [hp_X]/mL
- ANSER ANSER FEATHER 9 [hp_X]/mL
- ARSENIC TRIOXIDE 12 [hp_X]/mL - An inorganic compound with the chemical formula As2O3 that is used for the treatment of ACUTE PROMYELOCYTIC LEUKEMIA in patients who have relapsed from, or are resistant to, conventional drug therapy.
- BOS TAURUS SKIN 9 [hp_X]/mL
- CANIS LUPUS FAMILIARIS SKIN 9 [hp_X]/mL
- CAPRA HIRCUS SKIN 9 [hp_X]/mL
- CAVIA PORCELLUS SKIN 9 [hp_X]/mL
- EQUUS CABALLUS SKIN 9 [hp_X]/mL
- FELIS CATUS HAIR 9 [hp_X]/mL
- GALLUS GALLUS FEATHER 9 [hp_X]/mL
- MELOPSITTACUS UNDULATUS FEATHER 9 [hp_X]/mL
- MERIONES UNGUICULATUS SKIN 9 [hp_X]/mL
- MESOCRICETUS AURATUS SKIN 9 [hp_X]/mL
- MUS MUSCULUS SKIN 9 [hp_X]/mL
- ORYCTOLAGUS CUNICULUS SKIN 9 [hp_X]/mL
- PHOSPHORUS 12 [hp_X]/mL - A non-metal element that has the atomic symbol P, atomic number 15, and atomic weight 31. It is an essential element that takes part in a broad variety of biochemical reactions.
- RATTUS NORVEGICUS SKIN 9 [hp_X]/mL
- SERINUS CANARIA FEATHER 9 [hp_X]/mL
- STRYCHNOS NUX-VOMICA SEED 12 [hp_X]/mL
- SUS SCROFA SKIN 9 [hp_X]/mL
Which are Animal Antigens UNII Codes?
The UNII codes for the active ingredients in this product are:
- SERINUS CANARIA FEATHER (UNII: 9EL3384IQY)
- SERINUS CANARIA FEATHER (UNII: 9EL3384IQY) (Active Moiety)
- FELIS CATUS HAIR (UNII: 1564HD0N96)
- FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
- BOS TAURUS SKIN (UNII: 7J12CD6O9L)
- BOS TAURUS SKIN (UNII: 7J12CD6O9L) (Active Moiety)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV)
- GALLUS GALLUS FEATHER (UNII: 1FCM16V0FV) (Active Moiety)
- CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T)
- CANIS LUPUS FAMILIARIS SKIN (UNII: X2W7CLE97T) (Active Moiety)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796)
- ANAS PLATYRHYNCHOS FEATHER (UNII: 83B65P4796) (Active Moiety)
- MERIONES UNGUICULATUS SKIN (UNII: 9WN2H714TG)
- MERIONES UNGUICULATUS SKIN (UNII: 9WN2H714TG) (Active Moiety)
- CAPRA HIRCUS SKIN (UNII: JLG9853E2P)
- CAPRA HIRCUS SKIN (UNII: JLG9853E2P) (Active Moiety)
- ANSER ANSER FEATHER (UNII: 15XI414745)
- CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8)
- CAVIA PORCELLUS SKIN (UNII: GM3H4U6QS8) (Active Moiety)
- MESOCRICETUS AURATUS SKIN (UNII: 3K873H631W)
- MESOCRICETUS AURATUS SKIN (UNII: 3K873H631W) (Active Moiety)
- SUS SCROFA SKIN (UNII: 3EM4VW6TQN)
- SUS SCROFA SKIN (UNII: 3EM4VW6TQN) (Active Moiety)
- EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4)
- EQUUS CABALLUS SKIN (UNII: 88VZV9HGT4) (Active Moiety)
- MUS MUSCULUS SKIN (UNII: 390AN9GB09)
- MUS MUSCULUS SKIN (UNII: 390AN9GB09) (Active Moiety)
- MELOPSITTACUS UNDULATUS FEATHER (UNII: 1XY644QKWG)
- MELOPSITTACUS UNDULATUS FEATHER (UNII: 1XY644QKWG) (Active Moiety)
- ORYCTOLAGUS CUNICULUS SKIN (UNII: Z91WAU43WC)
- ORYCTOLAGUS CUNICULUS SKIN (UNII: Z91WAU43WC) (Active Moiety)
- RATTUS NORVEGICUS SKIN (UNII: Y69HPD48AI)
- RATTUS NORVEGICUS SKIN (UNII: Y69HPD48AI) (Active Moiety)
- ARSENIC TRIOXIDE (UNII: S7V92P67HO)
- ARSENIC CATION (3+) (UNII: C96613F5AV) (Active Moiety)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919)
- STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (Active Moiety)
- PHOSPHORUS (UNII: 27YLU75U4W)
- PHOSPHORUS (UNII: 27YLU75U4W) (Active Moiety)
Which are Animal Antigens 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)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Animal Antigens?
- Allergens - [CS]
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Cells, Epidermal - [EXT]
- Dander - [CS]
- Feathers - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Animal Skin Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Feather Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Salivary Proteins and Peptides - [CS]
- Seed Storage Proteins - [CS]
- Standardized Animal Hair Allergenic Extract - [EPC] (Established Pharmacologic Class)
* Please review the disclaimer below.
[1] What is the Non-Proprietary Name? - The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
[2] What is the Substance Name? - An active ingredient is the substance responsible for the medicinal effects of a product specified by the substance's molecular structure or if the molecular structure is not known, defined by an unambiguous definition that identifies the substance. Each active ingredient name is the preferred term of the UNII code submitted.
[3] What kind of product is this? - Indicates the type of product, such as Human Prescription Drug or Human Over the Counter Drug. This data element matches the “Document Type” field of the Structured Product Listing.
[4] What are the Administration Routes? - The translation of the route code submitted by the firm, indicating route of administration.
[5] What is the Labeler Name? - Name of Company corresponding to the labeler code segment of the Product NDC.
[8] What is the Marketing Category? - Product types are broken down into several potential Marketing Categories, such as NDA/ANDA/BLA, OTC Monograph, or Unapproved Drug. One and only one Marketing Category may be chosen for a product, not all marketing categories are available to all product types. Currently, only final marketed product categories are included. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.
[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".