NDC 43742-0575 Grain And Soy Allergen Mix

Adenosinum Triphosphoricum Acidum, Coumarinum, Quercetin, Rutin, Ileum (suis), Jejunum (suis), Stomach (suis), Bacillus Thuringiensis (bt Toxin), Bamboo, Barley, Eschscholzia Californica, Corn, Flax Seed, Gossypium Herbaceum, Millet, Milo, Avena Sativa, Oryza Sativa, Rye, Safflower, Sesamum, Sorghum Bicolor, Glycine Max, Saccharum, Helianthus Annuus, Wheat, Gluten, Amaranth, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Sycotic Co Bacillus

NDC Product Code 43742-0575

NDC Code: 43742-0575

Proprietary Name: Grain And Soy Allergen Mix What is the Proprietary Name?
The proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.

Non-Proprietary Name: Adenosinum Triphosphoricum Acidum, Coumarinum, Quercetin, Rutin, Ileum (suis), Jejunum (suis), Stomach (suis), Bacillus Thuringiensis (bt Toxin), Bamboo, Barley, Eschscholzia Californica, Corn, Flax Seed, Gossypium Herbaceum, Millet, Milo, Avena Sativa, Oryza Sativa, Rye, Safflower, Sesamum, Sorghum Bicolor, Glycine Max, Saccharum, Helianthus Annuus, Wheat, Gluten, Amaranth, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Sycotic Co Bacillus 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.

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.
    • 43742-0575 - Grain And Soy Allergen Mix

NDC 43742-0575-1

Package Description: 30 mL in 1 BOTTLE, DROPPER

NDC Product Information

Grain And Soy Allergen Mix with NDC 43742-0575 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Grain And Soy Allergen Mix is adenosinum triphosphoricum acidum, coumarinum, quercetin, rutin, ileum (suis), jejunum (suis), stomach (suis), bacillus thuringiensis (bt toxin), bamboo, barley, eschscholzia californica, corn, flax seed, gossypium herbaceum, millet, milo, avena sativa, oryza sativa, rye, safflower, sesamum, sorghum bicolor, glycine max, saccharum, helianthus annuus, wheat, gluten, amaranth, natrum sulphuricum, sarcolacticum acidum, triticum repens, adrenocorticotrophin, sycotic co bacillus. The product's dosage form is liquid and is administered via oral form.

Labeler Name: Deseret Biologicals, Inc.

Dosage Form: Liquid - A dosage form consisting of a pure chemical in its liquid1 state. This dosage form term should not be applied to solutions.

Product Type: Human Otc Drug 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.

Grain And Soy Allergen Mix Active Ingredient(s)

What is the Active Ingredient(s) List?
This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted.

  • ADENOSINE TRIPHOSPHATE DISODIUM 4 [hp_X]/mL
  • COUMARIN 6 [hp_X]/mL
  • QUERCETIN 6 [hp_X]/mL
  • RUTIN 6 [hp_X]/mL
  • SUS SCROFA ILEUM 8 [hp_X]/mL
  • SUS SCROFA JEJUNUM 8 [hp_X]/mL
  • SUS SCROFA STOMACH 8 [hp_X]/mL
  • THURINGIENSIN 8 [hp_X]/mL
  • BAMBUSA VULGARIS LEAF 9 [hp_X]/mL
  • BARLEY 9 [hp_X]/mL
  • ESCHSCHOLZIA CALIFORNICA 9 [hp_X]/mL
  • CORN 9 [hp_X]/mL
  • FLAX SEED 9 [hp_X]/mL
  • GOSSYPIUM HERBACEUM SEED RESIN 9 [hp_X]/mL
  • MILLET 9 [hp_X]/mL
  • SORGHUM BICOLOR WHOLE 9 [hp_X]/mL
  • AVENA SATIVA WHOLE 9 [hp_X]/mL
  • ORYZA SATIVA WHOLE 9 [hp_X]/mL
  • RYE 9 [hp_X]/mL
  • SAFFLOWER 9 [hp_X]/mL
  • SESAME SEED 9 [hp_X]/mL
  • GLYCINE MAX WHOLE 9 [hp_X]/mL
  • SACCHARUM OFFICINARUM WHOLE 9 [hp_X]/mL
  • HELIANTHUS ANNUUS FLOWERING TOP 9 [hp_X]/mL
  • WHEAT 9 [hp_X]/mL
  • WHEAT GLUTEN 30 [hp_C]/mL
  • AMARANTH 6 [hp_C]/mL
  • SODIUM SULFATE 6 [hp_C]/mL
  • LACTIC ACID, L- 6 [hp_C]/mL
  • ELYMUS REPENS ROOT 6 [hp_C]/mL
  • CORTICOTROPIN 8 [hp_C]/mL
  • ENTEROCOCCUS FAECALIS 30 [hp_C]/mL

Inactive Ingredient(s)

About the Inactive Ingredient(s)
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.

  • WATER (UNII: 059QF0KO0R)
  • ALCOHOL (UNII: 3K9958V90M)

Administration Route(s)

What are the Administration Route(s)?
The translation of the route code submitted by the firm, indicating route of administration.

  • Oral - Administration to or by way of the mouth.

Product Labeler Information

What is the Labeler Name?
Name of Company corresponding to the labeler code segment of the Product NDC.

Labeler Name: Deseret Biologicals, Inc.
Labeler Code: 43742
Marketing Category: UNAPPROVED HOMEOPATHIC - 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.

Start Marketing Date: 04-29-2015 What is the Start Marketing Date?
This is the date that the labeler indicates was the start of its marketing of the drug product.

End Marketing Date: 09-15-2020 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.

Exclude Flag: N 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. Values = ‘Y’ or ‘N’.

* Please review the disclaimer below.

Grain And Soy Allergen Mix Product Label Images

Grain And Soy Allergen Mix Product Labeling Information

The product labeling information includes all published material associated to a drug. Product labeling documents include information like generic names, active ingredients, ingredient strength dosage, routes of administration, appearance, usage, warnings, inactive ingredients, etc.

Product Labeling Index

Active Ingredients:

Adenosinum Triphosphoricum Acidum 4X, Coumarinum 6X, 8X, 10X, 30X, 200X, Quercetin 6X, 8X, 10X, 30X, 200X, Rutin 6X, 8X, 10X, 30X, 200X, Ileum (Suis) 8X, Jejunum (Suis) 8X, Stomach (Suis) 8X, Bacillus Thuringiensis (BT Toxin) 8X, 10X, 30X, 200X, Bamboo 9X, 12X, 15X, 30X, Barley 9X, 12X, 15X, 30X, Eschscholzia Californica 9X, 12X, 15X, 30X, Corn 9X, 12X, 15X, 30X, Flax Seed 9X, 12X, 15X, 30X, Gossypium Herbaceum 9X, 12X, 15X, 30X, Millet 9X, 12X, 15X, 30X, Milo 9X, 12X, 15X, 30X, Avena Sativa 9X, 12X, 15X, 30X, 6C, 30C, 200C, Oryza Sativa 9X, 12X, 15X, 30X, Rye 9X, 12X, 15X, 30X, Safflower 9X, 12X, 15X, 30X, Sesamum 9X, 12X, 15X, 30X, Sorghum Bicolor 9X, 12X, 15X, 30X, Glycine Max 9X, 12X, 15X, 30X, Saccharum 9X, 12X, 15X, 30X, Helianthus Annuus 9X, 12X, 15X, 30X, Wheat 9X, 12X, 15X, 30X, Gluten 30X, 200X, Amaranth 6C, 30C, 200C, Natrum Sulphuricum 6C, 30C, 200C, Sarcolacticum Acidum 6C, 30C, 200C, Triticum Repens 6C, 30C, 200C, Adrenocorticotrophin 8C, 30C, 200C, Sycotic Co Bacillus 30C, 200C.

Indications:

For the temporary relief of symptoms related to consumption of grains, soy, and gluten, including bowel irregularity, diarrhea, constipation, and fatigue.

For the temporary relief of symptoms related to consumption of grains, soy, and gluten, including bowel irregularity, diarrhea, constipation, and fatigue.

Warnings:

Keep out of reach of children. In case of overdose, contact a physician or 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.

Keep Out Of Reach Of Children:

Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

Directions:

3 to 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.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

Dist. By: Deseret Biologicals, Inc. 469 W. Parkland DriveSandy, UT 84070   www.desbio.com

Package Label Display:

DESBIONDC 43742-0575-1HOMEOPATHICGRAIN & SOYALLERGEN MIX1 FL OZ (30 ml)

* Please review the disclaimer below.

Previous Code
43742-0572
Next Code
43742-0576