NDC 43742-1627 Grain And Soy Allergen Mix
Adenosinum Triphosphoricum Dinatrum,Quercetin,Rutin,Natrum Carbonicum,Ileum (suis),Jejunum - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1627 - Grain And Soy Allergen Mix
Product Packages
NDC Code 43742-1627-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1627?
What are the uses for Grain And Soy Allergen Mix?
What are Grain And Soy Allergen Mix Active Ingredients?
- ADENOSINE TRIPHOSPHATE DISODIUM 4 [hp_X]/mL
- AMARANTH 6 [hp_C]/mL
- AVENA SATIVA FLOWERING TOP 6 [hp_C]/mL
- CORTISONE ACETATE 8 [hp_C]/mL - A naturally occurring glucocorticoid that has been used in replacement therapy for ADRENAL INSUFFICIENCY and as an anti-inflammatory agent. Cortisone itself is inactive; it is converted in the liver to the active metabolite HYDROCORTISONE. (From Martindale, The Extra Pharmacopoeia, 30th ed, p726)
- ELYMUS REPENS ROOT 6 [hp_C]/mL
- ENTEROCOCCUS FAECALIS 30 [hp_C]/mL - A species of gram-positive, coccoid bacteria commonly isolated from clinical specimens and the human intestinal tract. Most strains are nonhemolytic.
- GLYPHOSATE 12 [hp_C]/mL - Active compound in herbicidal formulations that inhibits 3-PHOSPHOSHIKIMATE 1-CARBOXYVINYLTRANSFERASE.
- LACTIC ACID, L- 6 [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.
- RUTIN 6 [hp_X]/mL - A flavonol glycoside found in many plants, including BUCKWHEAT; TOBACCO; FORSYTHIA; HYDRANGEA; VIOLA, etc. It has been used therapeutically to decrease capillary fragility.
- SODIUM CARBONATE 6 [hp_X]/mL
- SODIUM SULFATE 6 [hp_C]/mL
- SUS SCROFA ILEUM 8 [hp_X]/mL
- SUS SCROFA JEJUNUM 8 [hp_X]/mL
- SUS SCROFA STOMACH 8 [hp_X]/mL
- WHEAT GLUTEN 30 [hp_X]/mL
Which are Grain And Soy 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)
- QUERCETIN (UNII: 9IKM0I5T1E)
- QUERCETIN (UNII: 9IKM0I5T1E) (Active Moiety)
- RUTIN (UNII: 5G06TVY3R7)
- RUTIN (UNII: 5G06TVY3R7) (Active Moiety)
- SODIUM CARBONATE (UNII: 45P3261C7T)
- CARBONATE ION (UNII: 7UJQ5OPE7D) (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)
- WHEAT GLUTEN (UNII: 1534K8653J)
- WHEAT GLUTEN (UNII: 1534K8653J) (Active Moiety)
- AMARANTH (UNII: 37RBV3X49K)
- AMARANTH ACID (UNII: 02J7X17ZUQ) (Active Moiety)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F)
- AVENA SATIVA FLOWERING TOP (UNII: MA9CQJ3F7F) (Active Moiety)
- SODIUM SULFATE (UNII: 0YPR65R21J)
- SODIUM SULFATE ANHYDROUS (UNII: 36KCS0R750) (Active Moiety)
- LACTIC ACID, L- (UNII: F9S9FFU82N)
- LACTIC ACID, L- (UNII: F9S9FFU82N) (Active Moiety)
- ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W)
- ELYMUS REPENS ROOT (UNII: 3IXW0F6P8W) (Active Moiety)
- CORTISONE ACETATE (UNII: 883WKN7W8X)
- CORTISONE (UNII: V27W9254FZ) (Active Moiety)
- GLYPHOSATE (UNII: 4632WW1X5A)
- GLYPHOSATE (UNII: 4632WW1X5A) (Active Moiety)
- ENTEROCOCCUS FAECALIS (UNII: 15E04LZ9CT)
- ENTEROCOCCUS FAECALIS (UNII: 15E04LZ9CT) (Active Moiety)
Which are Grain And Soy 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 Grain And Soy Allergen Mix?
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Corticosteroid Hormone Receptor Agonists - [MoA] (Mechanism of Action)
- Corticosteroid - [EPC] (Established Pharmacologic Class)
- Dietary Proteins - [CS]
- Grain Proteins - [EXT]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Non-Standardized Food 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".