NDC 43742-1008 Gi Drainage

Cinnamomum, Gentiana Lutea, Syzygium Jambolanum, Argentum Nitricum, Colchicum Autumnale, Colostrum, Copper Gluconate, Lappa Major, Lycopodium Clavatum, Magnesium Gluconate, Manganese Gluconate, Nitricum Acidum, Pancreas Suis, Potassium Gluconate, Rumex Crispus, Schrophu8laria Nodosa, Stomach (suis), Aurum Metallicum, Beech, Calcarea Carbonica, Carbo Vegetabilis, Cherry Plum, Crab Apple, Intestine (suis), Rock Water, Fagus Sylvatica, Flos

  1. Labeler Index
  2. Deseret Biologicals, Inc.
  3. NDC: 43742-1008 Gi Drainage

NDC Product Code 43742-1008

NDC CODE: 43742-1008

Proprietary Name: Gi Drainage 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: Cinnamomum, Gentiana Lutea, Syzygium Jambolanum, Argentum Nitricum, Colchicum Autumnale, Colostrum, Copper Gluconate, Lappa Major, Lycopodium Clavatum, Magnesium Gluconate, Manganese Gluconate, Nitricum Acidum, Pancreas Suis, Potassium Gluconate, Rumex Crispus, Schrophu8laria Nodosa, Stomach (suis), Aurum Metallicum, Beech, Calcarea Carbonica, Carbo Vegetabilis, Cherry Plum, Crab Apple, Intestine (suis), Rock Water, Fagus Sylvatica, Flos 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
  • This medication is a mineral supplement used to prevent and treat low amounts of magnesium in the blood. Some brands are also used to treat symptoms of too much stomach acid such as stomach upset, heartburn, and acid indigestion. Magnesium is very important for the normal functioning of cells, nerves, muscles, bones, and the heart. Usually, a well-balanced diet provides normal blood levels of magnesium. However, certain situations cause your body to lose magnesium faster than you can replace it from your diet. These situations include treatment with water pills (diuretics such as furosemide, hydrochlorothiazide), a poor diet, alcoholism, or other medical conditions (e.g., severe diarrhea/vomiting, stomach/intestinal absorption problems, poorly controlled diabetes).
  • Drug uses not available

NDC Code Structure

  • 43742 - Deseret Biologicals, Inc.

NDC 43742-1008-1

Package Description: 60 mL in 1 BOTTLE, DROPPER

NDC Product Information

Gi Drainage with NDC 43742-1008 is a a human over the counter drug product labeled by Deseret Biologicals, Inc.. The generic name of Gi Drainage is cinnamomum, gentiana lutea, syzygium jambolanum, argentum nitricum, colchicum autumnale, colostrum, copper gluconate, lappa major, lycopodium clavatum, magnesium gluconate, manganese gluconate, nitricum acidum, pancreas suis, potassium gluconate, rumex crispus, schrophu8laria nodosa, stomach (suis), aurum metallicum, beech, calcarea carbonica, carbo vegetabilis, cherry plum, crab apple, intestine (suis), rock water, fagus sylvatica, flos. 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.

Gi Drainage 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.
  • CINNAMON 3 [hp_X]/mL
  • GENTIANA LUTEA ROOT 3 [hp_X]/mL
  • SYZYGIUM CUMINI SEED 3 [hp_X]/mL
  • SILVER NITRATE 6 [hp_X]/mL
  • COLCHICUM AUTUMNALE BULB 6 [hp_X]/mL
  • BOS TAURUS COLOSTRUM 6 [hp_X]/mL
  • COPPER GLUCONATE 6 [hp_X]/mL
  • ARCTIUM LAPPA ROOT 6 [hp_X]/mL
  • LYCOPODIUM CLAVATUM SPORE 6 [hp_X]/mL
  • MAGNESIUM GLUCONATE 6 [hp_X]/mL
  • MANGANESE GLUCONATE 6 [hp_X]/mL
  • NITRIC ACID 6 [hp_X]/mL
  • SUS SCROFA PANCREAS 6 [hp_X]/mL
  • POTASSIUM GLUCONATE 6 [hp_X]/mL
  • RUMEX CRISPUS ROOT 6 [hp_X]/mL
  • SCROPHULARIA NODOSA 6 [hp_X]/mL
  • SUS SCROFA STOMACH 6 [hp_X]/mL
  • GOLD 8 [hp_X]/mL
  • OYSTER SHELL CALCIUM CARBONATE, CRUDE 8 [hp_X]/mL
  • ACTIVATED CHARCOAL 8 [hp_X]/mL
  • PORK INTESTINE 8 [hp_X]/mL
  • MALUS PUMILA FLOWER 8 [hp_X]/mL
  • PRUNUS CERASIFERA FLOWER 8 [hp_X]/mL
  • FAGUS SYLVATICA FLOWERING TOP 12 [hp_X]/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: 05-19-2017 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: 07-19-2023 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.

Gi Drainage Product Label Images

Gi Drainage 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:

Cinnamomum 3X, Gentiana Lutea 3X, Syzygium Jambolanum 3X, Argentum Nitricum 6X, Colchicum Autumnale 6X, Colostrum 6X, Copper Gluconate 6X, Lappa Major 6X, Lycopodium Clavatum 6X, Magnesium Gluconate 6X, Manganese Gluconate 6X, Nitricum Acidum 6X, Pancreas Suis 6X, Potassium Gluconate 6X, Rumex Crispus 6X, Scrophularia Nodosa 6X, Stomach (Suis) 6X, Aurum Metallicum 8X, Fagus Sylvatica, Flos 8X, Calcarea Carbonica 8X, Carbo Vegetabilis 8X, Malus Pumila, Flos 8X, Prunus Cerasifera, Flos 8X, Intestine (Suis) 8X, Rock Water 8X, Fagus Sylvatica, Flos 12X.

Homeopathic Indications:

For the temporary relief of the symptoms related to the detoxification and cleansing of the gastrointestinal tract, such as fatigue, irregularity and low energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

For the temporary relief of the symptoms related to the detoxification and cleansing of the gastrointestinal tract, such as fatigue, irregularity and low energy.****These statements are based upon traditional homeopathic principles. They have not been reviewed by the Food and Drug Administration.

Warnings:

Keep out of reach of children. In case of overdose, contact 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, contact physician or Poison Control Center right away.

Directions:

1-10 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 43742-1008-1HOMEOPATHICGI DRAINAGE2 FL OZ (60 ml)

* Please review the disclaimer below.