NDC 43742-1417 Grain And Soy Allergen Mix
Adenosinum Triphosphoricum Dinatrum,Quercetin,Rutin,Ileum (suis),Jejunum (suis) Stomach - View Dosage, Usage, Ingredients, Routes, UNII
Product Information
- 43742 - Deseret Biologicals, Inc.
- 43742-1417 - Grain And Soy Allergen Mix
Product Packages
NDC Code 43742-1417-1
Package Description: 30 mL in 1 BOTTLE, DROPPER
Product Details
What is NDC 43742-1417?
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
- BACILLUS THURINGIENSIS 10 [hp_X]/mL - A species of gram-positive bacteria which may be pathogenic for certain insects. It is used for the biological control of the Gypsy moth.
- BAMBUSA VULGARIS LEAF 9 [hp_X]/mL
- BARLEY 9 [hp_X]/mL
- BROWN RICE 9 [hp_X]/mL
- CORN 9 [hp_X]/mL
- CORTICOTROPIN 8 [hp_C]/mL
- 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.
- FLAX SEED 9 [hp_X]/mL
- GLYPHOSATE 12 [hp_C]/mL - Active compound in herbicidal formulations that inhibits 3-PHOSPHOSHIKIMATE 1-CARBOXYVINYLTRANSFERASE.
- LACTIC ACID, L- 6 [hp_C]/mL
- LEVANT COTTON SEED 9 [hp_X]/mL
- MILLET 9 [hp_X]/mL - An agronomic group especially of small-seeded grasses, mainly grown for human and animal consumption.
- OAT 9 [hp_X]/mL - Oats, genus of the family POACEAE.
- POPPY SEED 9 [hp_X]/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.
- RYE 9 [hp_X]/mL
- SAFFLOWER 9 [hp_X]/mL
- SESAME SEED 9 [hp_X]/mL
- SODIUM SULFATE 6 [hp_C]/mL
- SORGHUM 9 [hp_X]/mL - A plant genus of the family POACEAE. The grain is used for FOOD and for ANIMAL FEED. This should not be confused with KAFFIR LIME or with KEFIR milk product.
- SORGHUM BICOLOR WHOLE 9 [hp_X]/mL
- SOYBEAN 9 [hp_X]/mL - An annual legume. The SEEDS of this plant are edible and used to produce a variety of SOY FOODS.
- SUGARCANE 9 [hp_X]/mL
- SUNFLOWER SEED 9 [hp_X]/mL
- SUS SCROFA ILEUM 8 [hp_X]/mL
- SUS SCROFA JEJUNUM 8 [hp_X]/mL
- SUS SCROFA STOMACH 8 [hp_X]/mL
- WHEAT 9 [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)
- 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)
- BAMBUSA VULGARIS LEAF (UNII: EMY54R518C)
- BAMBUSA VULGARIS LEAF (UNII: EMY54R518C) (Active Moiety)
- BARLEY (UNII: 5PWM7YLI7R)
- BARLEY (UNII: 5PWM7YLI7R) (Active Moiety)
- POPPY SEED (UNII: 60RO23IR87)
- POPPY SEED (UNII: 60RO23IR87) (Active Moiety)
- CORN (UNII: 0N8672707O)
- CORN (UNII: 0N8672707O) (Active Moiety)
- FLAX SEED (UNII: 4110YT348C)
- FLAX SEED (UNII: 4110YT348C) (Active Moiety)
- LEVANT COTTON SEED (UNII: 550E4N439V)
- LEVANT COTTON SEED (UNII: 550E4N439V) (Active Moiety)
- MILLET (UNII: TJR6B3R47P)
- MILLET (UNII: TJR6B3R47P) (Active Moiety)
- SORGHUM BICOLOR WHOLE (UNII: Y3T98X3AL6)
- SORGHUM BICOLOR WHOLE (UNII: Y3T98X3AL6) (Active Moiety)
- OAT (UNII: Z6J799EAJK)
- OAT (UNII: Z6J799EAJK) (Active Moiety)
- BROWN RICE (UNII: 659G217HPG)
- BROWN RICE (UNII: 659G217HPG) (Active Moiety)
- RYE (UNII: 0R4AQI398X)
- RYE (UNII: 0R4AQI398X) (Active Moiety)
- SAFFLOWER (UNII: 4VBL71TY4Y)
- SAFFLOWER (UNII: 4VBL71TY4Y) (Active Moiety)
- SESAME SEED (UNII: 7Y1255HVXR)
- SESAME SEED (UNII: 7Y1255HVXR) (Active Moiety)
- SORGHUM (UNII: CUL9PN8ELJ)
- SORGHUM (UNII: CUL9PN8ELJ) (Active Moiety)
- SOYBEAN (UNII: L7HT8F1ZOD)
- SOYBEAN (UNII: L7HT8F1ZOD) (Active Moiety)
- SUGARCANE (UNII: 81H2R5AOH3)
- SUGARCANE (UNII: 81H2R5AOH3) (Active Moiety)
- SUNFLOWER SEED (UNII: R9N3379M4Z)
- SUNFLOWER SEED (UNII: R9N3379M4Z) (Active Moiety)
- WHEAT (UNII: 4J2I0SN84Y)
- WHEAT (UNII: 4J2I0SN84Y) (Active Moiety)
- BACILLUS THURINGIENSIS (UNII: 3TK3LQP1N7)
- BACILLUS THURINGIENSIS (UNII: 3TK3LQP1N7) (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)
- CORTICOTROPIN (UNII: K0U68Q2TXA)
- CORTICOTROPIN (UNII: K0U68Q2TXA) (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?
- Adrenocorticotropic Hormone - [CS]
- Adrenocorticotropic Hormone - [EPC] (Established Pharmacologic Class)
- Allergens - [CS]
- Cell-mediated Immunity - [PE] (Physiologic Effect)
- Dietary Proteins - [CS]
- Grain Proteins - [EXT]
- Increased Histamine Release - [PE] (Physiologic Effect)
- Increased IgG Production - [PE] (Physiologic Effect)
- Non-Standardized Food Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Non-Standardized Plant Allergenic Extract - [EPC] (Established Pharmacologic Class)
- Plant Proteins - [CS]
- Seed Storage Proteins - [CS]
- Vegetable Proteins - [CS]
* 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.
[7] What is the Drug Enforcement Administration (DEA) CII Schedule? - This is the assigned DEA Schedule number as reported by the labeler. Values are CI, CII, CIII, CIV, and CV.
[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".