Grain And Soy Allergen Mix

Adenosinum Triphosphoricum Dinatrum, Quercetin, Rutin, Ileum (suis), Jejunum (suis) Stomach (suis), Coumarinum, Bamboo, Barley, Poppy Seed, Corn, Flax Seed, Cotton Seed, Millet, Milo, Oat, Rice, Rye, Safflower, Sesame, Sorghum, Soy Bean, Sugarcane, Sunflower, Wheat, Bacillus Thuringiensis (bt Toxin), Gluten, Amaranth, Avena Sativa, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Glyphosate, Sycotic Co Bacillus

Deseret Biologicals, Inc.
Human Otc Drug
NDC 43742-1292

Grain And Soy Allergen Mix also known as Adenosinum Triphosphoricum Dinatrum, Quercetin, Rutin, Ileum (suis), Jejunum (suis) Stomach (suis), Coumarinum, Bamboo, Barley, Poppy Seed, Corn, Flax Seed, Cotton Seed, Millet, Milo, Oat, Rice, Rye, Safflower, Sesame, Sorghum, Soy Bean, Sugarcane, Sunflower, Wheat, Bacillus Thuringiensis (bt Toxin), Gluten, Amaranth, Avena Sativa, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Glyphosate, Sycotic Co Bacillus is a human otc drug labeled by 'Deseret Biologicals, Inc.'. National Drug Code (NDC) number for Grain And Soy Allergen Mix is 43742-1292. This drug is available in dosage form of Liquid. The names of the active, medicinal ingredients in Grain And Soy Allergen Mix drug includes 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 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 Coumarin - 8 [hp_X]/mL and more. The currest status of Grain And Soy Allergen Mix drug is Active.

Drug Information:

Drug NDC:	43742-1292
The labeler code and product code segments of the National Drug Code number, separated by a hyphen. Asterisks are no longer used or included within the product code segment to indicate certain configurations of the NDC.
Proprietary Name:	Grain And Soy Allergen Mix
Also known as the trade name. It is the name of the product chosen by the labeler.
Product Type:	Human Otc Drug
Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing.
Non Proprietary Name:	Adenosinum Triphosphoricum Dinatrum, Quercetin, Rutin, Ileum (suis), Jejunum (suis) Stomach (suis), Coumarinum, Bamboo, Barley, Poppy Seed, Corn, Flax Seed, Cotton Seed, Millet, Milo, Oat, Rice, Rye, Safflower, Sesame, Sorghum, Soy Bean, Sugarcane, Sunflower, Wheat, Bacillus Thuringiensis (bt Toxin), Gluten, Amaranth, Avena Sativa, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Glyphosate, Sycotic Co Bacillus
Also known as the generic name, this is usually the active ingredient(s) of the product.
Labeler Name:	Deseret Biologicals, Inc.
Name of Company corresponding to the labeler code segment of the ProductNDC.
Dosage Form:	Liquid
The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources.
Status:	Active
FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved.
Substance Name:	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 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 COUMARIN - 8 [hp_X]/mL Load more... ELYMUS REPENS ROOT - 6 [hp_C]/mL ENTEROCOCCUS FAECALIS - 30 [hp_C]/mL FLAX SEED - 9 [hp_X]/mL GLYPHOSATE - 12 [hp_C]/mL LACTIC ACID, L- - 6 [hp_C]/mL LEVANT COTTON SEED - 9 [hp_X]/mL MILLET - 9 [hp_X]/mL OAT - 9 [hp_X]/mL POPPY SEED - 9 [hp_X]/mL QUERCETIN - 6 [hp_X]/mL RUTIN - 6 [hp_X]/mL 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 SORGHUM BICOLOR WHOLE - 9 [hp_X]/mL SOYBEAN - 9 [hp_X]/mL 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
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.
Route Details:	ORAL
The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources.

Marketing Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Marketing Category:	UNAPPROVED HOMEOPATHIC
Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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.
Marketing Start Date:	27 Jul, 2018
This is the date that the labeler indicates was the start of its marketing of the drug product.
Marketing End Date:	14 Aug, 2023
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.
Listing Expiration Date:	23 Dec, 2025
This is the date when the listing record will expire if not updated or certified by the firm.

OpenFDA Information:

An openfda section: An annotation with additional product identifiers, such as NUII and UPC, of the drug product, if available.

Manufacturer Name:	Deseret Biologicals, Inc.
Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC.
Original Packager:	Yes
Whether or not the drug has been repackaged for distribution.
NUI:	N0000185371 N0000175629 N0000184306 M0000728 M0006342 N0000185016 M0000499 N0000175941 N0000185375 N0000185001 M0016962 M0516536 M0022575
Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT).
UNII:	5L51B4DR1G 37RBV3X49K MA9CQJ3F7F 3TK3LQP1N7 EMY54R518C 5PWM7YLI7R 659G217HPG 0N8672707O K0U68Q2TXA A4VZ22K1WT Load more... 3IXW0F6P8W 15E04LZ9CT 4110YT348C 4632WW1X5A F9S9FFU82N 550E4N439V TJR6B3R47P Z6J799EAJK 60RO23IR87 9IKM0I5T1E 5G06TVY3R7 0R4AQI398X 4VBL71TY4Y 7Y1255HVXR 0YPR65R21J CUL9PN8ELJ Y3T98X3AL6 L7HT8F1ZOD 81H2R5AOH3 R9N3379M4Z C998R1XSRA TA501QD69R T0920P9Z9A 4J2I0SN84Y 1534K8653J
Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information.
Pharmacologic Class EPC:	Non-Standardized Food Allergenic Extract [EPC] Adrenocorticotropic Hormone [EPC] Non-Standardized Plant Allergenic Extract [EPC]
Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`.
Pharmacologic Class PE:	Increased Histamine Release [PE] Cell-mediated Immunity [PE] Increased IgG Production [PE]
Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`.
Pharmacologic Class CS:	Allergens [CS] Dietary Proteins [CS] Adrenocorticotropic Hormone [CS] Plant Proteins [CS] Seed Storage Proteins [CS] Vegetable Proteins [CS]
Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient].
Pharmacologic Class:	Adrenocorticotropic Hormone [CS] Adrenocorticotropic Hormone [EPC] Allergens [CS] Cell-mediated Immunity [PE] Dietary Proteins [CS] Grain Proteins [EXT] Increased Histamine Release [PE] Increased IgG Production [PE] Non-Standardized Food Allergenic Extract [EPC] Non-Standardized Plant Allergenic Extract [EPC] Plant Proteins [CS] Seed Storage Proteins [CS] Vegetable Proteins [CS]
These are the reported pharmacological class categories corresponding to the SubstanceNames listed above.

Packaging Information:

Package NDC	Description	Marketing Start Date	Marketing End Date	Sample Available
43742-1292-1	30 mL in 1 BOTTLE, DROPPER (43742-1292-1)	27 Jul, 2018	14 Aug, 2023	No
Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together.

Other medicines with the same generic name

Grain And Soy Allergen Mix

Adenosinum Triphosphoricum Dinatrum & more..

Liquid
Deseret Biologicals, Inc.
NDC: 43742-1292

Purpose:

Homeopathic indications: for the temporary relief of symptoms related to consumption of grains, soy, and gluten, including bowel irregularity, occasional diarrhea, occasional constipation, and fatigue.** **these statements are based upon traditional homeopathic principles. they have not been reviewed by the food and drug administration.

Product Elements:

Grain and soy allergen mix adenosinum triphosphoricum dinatrum, quercetin, rutin, ileum (suis), jejunum (suis) stomach (suis), coumarinum, bamboo, barley, poppy seed, corn, flax seed, cotton seed, millet, milo, oat, rice, rye, safflower, sesame, sorghum, soy bean, sugarcane, sunflower, wheat, bacillus thuringiensis (bt toxin), gluten, amaranth, avena sativa, natrum sulphuricum, sarcolacticum acidum, triticum repens, adrenocorticotrophin, glyphosate, sycotic co bacillus adenosine triphosphate disodium adenosine triphosphate quercetin quercetin rutin rutin sus scrofa ileum sus scrofa ileum sus scrofa jejunum sus scrofa jejunum sus scrofa stomach sus scrofa stomach coumarin coumarin bambusa vulgaris leaf bambusa vulgaris leaf barley barley poppy seed poppy seed corn corn flax seed flax seed levant cotton seed levant cotton seed millet millet sorghum bicolor whole sorghum bicolor whole oat oat brown rice brown rice rye rye safflower safflower sesame seed sesame seed sorghum sorghum soybean soybean sugarcane sugarcane sunflower seed sunflower seed wheat wheat bacillus thuringiensis wheat gluten wheat gluten wheat gluten amaranth amaranth acid avena sativa flowering top avena sativa flowering top sodium sulfate sodium sulfate anhydrous lactic acid, l- lactic acid, l- elymus repens root elymus repens root corticotropin corticotropin glyphosate glyphosate enterococcus faecalis enterococcus faecalis water alcohol

Indications and Usage:

Warnings:

Warnings: keep out of reach of children. in case of overdose, contact physician or a poison control center right away. if pregnant or breast-feeding, ask a health professional before use. tamper seal: "sealed for your protection." do not use if seal is broken or missing.

Dosage and Administration:

Directions: 3-10 drops under the tongue, 3 times a day or as directed by a health professional. consult a physician for use in children under 12 years of age.

Package Label Principal Display Panel:

Package label display: des bio ndc 43742-1292-1 homeopathic grain & soy allergen mix 1 fl oz (30 ml) grain & soy allergen mix

Further Questions:

Questions: dist. by: deseret biologicals, inc. 469 w. parkland drive sandy, ut 84070 www.desbio.com

Comments/ Reviews:

* Data of this site is collected from www.fda.gov. This page is for informational purposes only. Always consult your physician with any questions you may have regarding a medical condition.