NDC 43742-1644 Egg Allergen Mix
Adenosinum Triphosphoricum Dinatrum,L-asparagine - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1644 - Egg Allergen Mix
Product Packages
NDC Code 43742-1644-1
Package Description: 30 mL in 1 PACKAGE
Product Details
What is NDC 43742-1644?
What are the uses for Egg Allergen Mix?
What are Egg Allergen Mix Active Ingredients?
- ADENOSINE TRIPHOSPHATE DISODIUM 4 [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
- EGG 28 [hp_C]/mL
- FERROUS IODIDE 6 [hp_C]/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.
- SUS SCROFA ILEUM 8 [hp_X]/mL
- SUS SCROFA JEJUNUM 8 [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)
- 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]
- Ascorbic Acid - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Egg Proteins, Dietary - [CS]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food 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.
[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".