NDC 43742-0578 Egg Allergen Mix
Adenosinum Triphosphoricum Dinatrum,L-asparagine - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-0578 - Egg Allergen Mix
Product Packages
NDC Code 43742-0578-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-0578?
What are the uses for Egg Allergen Mix?
What are Egg Allergen Mix Active Ingredients?
- ADENOSINE TRIPHOSPHATE DISODIUM 4 [hp_X]/mL
- ANAS PLATYRHYNCHOS FEATHER 9 [hp_X]/mL
- ANSER ANSER FEATHER 9 [hp_X]/mL
- ASCORBIC ACID 6 [hp_C]/mL - A six carbon compound related to glucose. It is found naturally in citrus fruits and many vegetables. Ascorbic acid is an essential nutrient in human diets, and necessary to maintain connective tissue and bone. Its biologically active form, vitamin C, functions as a reducing agent and coenzyme in several metabolic pathways. Vitamin C is considered an antioxidant.
- ASPARAGINE MONOHYDRATE 6 [hp_X]/mL
- 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
- EGG 28 [hp_C]/mL
- EQUUS CABALLUS SKIN 9 [hp_X]/mL
- FELIS CATUS HAIR 9 [hp_X]/mL
- FERROUS IODIDE 6 [hp_C]/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
- OYSTER SHELL CALCIUM CARBONATE, CRUDE 6 [hp_C]/mL
- PHENYLALANINE 6 [hp_X]/mL - An essential aromatic amino acid that is a precursor of MELANIN; DOPAMINE; noradrenalin (NOREPINEPHRINE), and THYROXINE.
- PROTEUS MORGANII 30 [hp_C]/mL
- QUERCETIN 6 [hp_X]/mL - A flavonol widely distributed in plants. It is an antioxidant, like many other phenolic heterocyclic compounds. Glycosylated forms include RUTIN and quercetrin.
- RATTUS NORVEGICUS SKIN 9 [hp_X]/mL
- SERINUS CANARIA FEATHER 9 [hp_X]/mL
- SUS SCROFA ILEUM 8 [hp_X]/mL
- SUS SCROFA JEJUNUM 8 [hp_X]/mL
- SUS SCROFA SKIN 9 [hp_X]/mL
- SUS SCROFA STOMACH 8 [hp_X]/mL
- TETRACYCLINE 6 [hp_C]/mL - A naphthacene antibiotic that inhibits AMINO ACYL TRNA binding during protein synthesis.
Which are Egg Allergen Mix UNII Codes?
The UNII codes for the active ingredients in this product are:
- ADENOSINE TRIPHOSPHATE DISODIUM (UNII: 5L51B4DR1G)
- ADENOSINE TRIPHOSPHATE (UNII: 8L70Q75FXE) (Active Moiety)
- ASPARAGINE MONOHYDRATE (UNII: 2PD79VF521)
- ASPARAGINE (UNII: 5Z33R5TKO7) (Active Moiety)
- PHENYLALANINE (UNII: 47E5O17Y3R)
- PHENYLALANINE (UNII: 47E5O17Y3R) (Active Moiety)
- QUERCETIN (UNII: 9IKM0I5T1E)
- QUERCETIN (UNII: 9IKM0I5T1E) (Active Moiety)
- SUS SCROFA ILEUM (UNII: C998R1XSRA)
- SUS SCROFA ILEUM (UNII: C998R1XSRA) (Active Moiety)
- SUS SCROFA JEJUNUM (UNII: TA501QD69R)
- SUS SCROFA JEJUNUM (UNII: TA501QD69R) (Active Moiety)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A)
- SUS SCROFA STOMACH (UNII: T0920P9Z9A) (Active Moiety)
- SERINUS CANARIA FEATHER (UNII: 9EL3384IQY)
- SERINUS CANARIA FEATHER (UNII: 9EL3384IQY) (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)
- FELIS CATUS HAIR (UNII: 1564HD0N96)
- FELIS CATUS HAIR (UNII: 1564HD0N96) (Active Moiety)
- ASCORBIC ACID (UNII: PQ6CK8PD0R)
- ASCORBIC ACID (UNII: PQ6CK8PD0R) (Active Moiety)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I)
- OYSTER SHELL CALCIUM CARBONATE, CRUDE (UNII: 2E32821G6I) (Active Moiety)
- FERROUS IODIDE (UNII: F5452U54PN)
- FERROUS IODIDE (UNII: F5452U54PN) (Active Moiety)
- TETRACYCLINE (UNII: F8VB5M810T)
- TETRACYCLINE (UNII: F8VB5M810T) (Active Moiety)
- EGG (UNII: 291P45F896)
- EGG (UNII: 291P45F896) (Active Moiety)
- PROTEUS MORGANII (UNII: 56X6LID5ZY)
- PROTEUS MORGANII (UNII: 56X6LID5ZY) (Active Moiety)
Which are Egg Allergen 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:
- WATER (UNII: 059QF0KO0R)
- ALCOHOL (UNII: 3K9958V90M)
Which are the Pharmacologic Classes for Egg Allergen Mix?
- Allergens - [CS]
- Allergens - [CS]
- Ascorbic Acid - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Cells, Epidermal - [EXT]
- Dander - [CS]
- Dietary Proteins - [CS]
- Egg Proteins, Dietary - [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 Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Salivary Proteins and Peptides - [CS]
- Standardized Animal Hair Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Tetracycline-class Antimicrobial - [EPC] (Established Pharmacologic Class)
- Tetracyclines - [CS]
- Vitamin C - [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.
[10] What is the End Marketing Date? - This is the date the product will no longer be available on the market. If a product is no longer being manufactured, in most cases, the FDA recommends firms use the expiration date of the last lot produced as the EndMarketingDate, to reflect the potential for drug product to remain available after manufacturing has ceased. Products that are the subject of ongoing manufacturing will not ordinarily have any EndMarketingDate. Products with a value in the EndMarketingDate will be removed from the NDC Directory when the EndMarketingDate is reached.
[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".