NDC 43742-0820 Grain Mix System Formula

Coumarinum, Quercetin, Rutin, Bamboo, Barley, Poppy Seed, Corn, Flax Seed, Cotton Seed, Millet, Milo, Oat, Rice, Rye, Safflower, Sesame, Sorghum, Soy Bean, Sugarcane, Sunflower, Wheat, Amaranth, Avena Sativa, Natrum Sulphuricum, Sarcolacticum Acidum, Triticum Repens, Adrenocorticotrophin, Sycotic Co Bacillus

NDC Product Code 43742-0820

NDC CODE: 43742-0820

Proprietary Name: Grain Mix System Formula 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: Coumarinum, Quercetin, Rutin, Bamboo, Barley, Poppy Seed, Corn, Flax Seed, Cotton Seed, Millet, Milo, Oat, Rice, Rye, Safflower, Sesame, Sorghum, Soy Bean, Sugarcane, Sunflower, Wheat, Amaranth, Avena Sativa, 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.

Drug Use Information

Drug Use Information
The drug use information is a summary and does NOT have all possible information about this product. This information does not assure that this product is safe, effective, or appropriate. This information is not individual medical advice and does not substitute for the advice of a health care professional. Always ask a health care professional for complete information about this product and your specific health needs.

  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-0820-1

Package Description: 30 mL in 1 PACKAGE

NDC Product Information

Grain Mix System Formula with NDC 43742-0820 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Grain Mix System Formula is coumarinum, quercetin, rutin, bamboo, barley, poppy seed, corn, flax seed, cotton seed, millet, milo, oat, rice, rye, safflower, sesame, sorghum, soy bean, sugarcane, sunflower, wheat, amaranth, avena sativa, 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 Mix System Formula 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.

  • COUMARIN 6 [hp_X]/mL
  • QUERCETIN 6 [hp_X]/mL
  • RUTIN 6 [hp_X]/mL
  • BAMBUSA VULGARIS LEAF 9 [hp_X]/mL
  • BARLEY 9 [hp_X]/mL
  • POPPY SEED 9 [hp_X]/mL
  • CORN 9 [hp_X]/mL
  • FLAX SEED 9 [hp_X]/mL
  • LEVANT COTTON SEED 9 [hp_X]/mL
  • MILLET 9 [hp_X]/mL
  • SORGHUM BICOLOR WHOLE 9 [hp_X]/mL
  • OAT 9 [hp_X]/mL
  • BROWN RICE 9 [hp_X]/mL
  • RYE 9 [hp_X]/mL
  • SAFFLOWER 9 [hp_X]/mL
  • SESAME SEED 9 [hp_X]/mL
  • SORGHUM 9 [hp_X]/mL
  • SOYBEAN 9 [hp_X]/mL
  • SUGARCANE 9 [hp_X]/mL
  • SUNFLOWER SEED 9 [hp_X]/mL
  • WHEAT 9 [hp_X]/mL
  • AMARANTH 6 [hp_C]/mL
  • AVENA SATIVA FLOWERING TOP 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.
  • 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: 07-21-2016 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: 11-20-2022 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 Mix System Formula 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:

Coumarinum 6X, 8X, 10X, 30X, 200X, Quercetin 6X, 8X, 10X, 30X, 200X, Rutin 6X, 8X, 10X, 30X, 200X, Bamboo 9X, 12X, 15X, 30X, Barley 9X, 12X, 15X, 30X, Poppy Seed 9X, 12X, 15X, 30X, Corn 9X, 12X, 15X, 30X, Flax Seed 9X, 12X, 15X, 30X, Cotton Seed 9X, 12X, 15X, 30X, Millet 9X, 12X, 15X, 30X, Milo 9X, 12X, 15X, 30X, Oat 9X, 12X, 15X, 30X, Rice 9X, 12X, 15X, 30X, Rye 9X, 12X, 15X, 30X, Safflower 9X, 12X, 15X, 30X, Sesame 9X, 12X, 15X, 30X, Sorghum 9X, 12X, 15X, 30X, Soy Bean 9X, 12X, 15X, 30X, Sugarcane 9X, 12X, 15X, 30X, Sunflower 9X, 12X, 15X, 30X, Wheat 9X, 12X, 15X, 30X, Amaranth 6C, 30C, 200C, Avena Sativa 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.

Homeopathic Indications:

Temporary relief of symptoms related to grains and gluten, including bowel irregularity, diarrhea, constipation and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Temporary relief of symptoms related to grains and gluten, including bowel irregularity, diarrhea, constipation and fatigue.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

If pregnant or breast-feeding, or have any allergic reaction to trace minerals, or any chronic or recurring symptoms or illness, consult a health professional before use.Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.Do not use if tamper evident seal is broken or missing.Store at room temperature.Keep out of direct sunlight.

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:

Adults 3-10 drops under the tongue 3 times daily or as directed by your health professional. Consult a physician for use in children under 12 years of age.

Inactive Ingredients:

Demineralized Water, 25% Ethanol

Questions:

DISTRIBUTED BY:Deseret Biologicals, Inc., Sandy, UT 84070800.827.9529     www.desbio.com

Package Label Display:

NAMBUDRIPAD'S ALLERGY ELIMINATION TECHNIQUESNAETNDC 43742-0820-1HOMEOPATHICGRAIN MIXSystem FormulaNet Contents 1 FL OZ (30 ML)DESBIO

* Please review the disclaimer below.