43742-1479 NDC - GI DRAINAGE (CINNAMOMUM, GENTIANA LUTEA, SYZYGIUM JAMBOLANUM, ARGENTUM NITRICUM, COLCHICUM AUTUMNALE, COLOSTRUM, COPPER GLUCONATE, LAPPA MAJOR, LYCOPODIUM CLAVATUM, MAGNESIUM GLUCONATE, MANGANESE GLUCONATE, POTASSIUM GLUCONATE, RUMEX CRISPUS, SCROPHULARIA NODOSA, STOMACH (SUIS), AURUM METALLICUM, CALCAREA CARBONICA, CARBO VEGETABILIS, INTESTINE (SUIS), MALUS PUMILA, FLOS, NITRICUM ACIDUM, PRUNUS CERASIFERA, FLOS, ROCK WATER, FAGUS SYLVATICA, FLOS)

Drug Information

Product NDC: 43742-1479

Proprietary Name: GI Drainage

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

Active Ingredient(s):
  • 8 [hp_X]/mL ACTIVATED CHARCOAL;
  • 6 [hp_X]/mL ARCTIUM LAPPA ROOT;
  • 6 [hp_X]/mL BOS TAURUS COLOSTRUM;
  • 3 [hp_X]/mL CINNAMON;
  • 6 [hp_X]/mL COLCHICUM AUTUMNALE BULB;
  • 6 [hp_X]/mL COPPER GLUCONATE;
  • 12 [hp_X]/mL FAGUS SYLVATICA FLOWERING TOP;
  • 3 [hp_X]/mL GENTIANA LUTEA ROOT;
  • 8 [hp_X]/mL GOLD;
  • 6 [hp_X]/mL LYCOPODIUM CLAVATUM SPORE;
  • 6 [hp_X]/mL MAGNESIUM GLUCONATE;
  • 8 [hp_X]/mL MALUS PUMILA FLOWER;
  • 6 [hp_X]/mL MANGANESE GLUCONATE;
  • 8 [hp_X]/mL NITRIC ACID;
  • 8 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE;
  • 8 [hp_X]/mL PORK INTESTINE;
  • 6 [hp_X]/mL POTASSIUM GLUCONATE;
  • 8 [hp_X]/mL PRUNUS CERASIFERA FLOWER;
  • 6 [hp_X]/mL RUMEX CRISPUS ROOT;
  • 6 [hp_X]/mL SCROPHULARIA NODOSA;
  • 6 [hp_X]/mL SILVER NITRATE;
  • 6 [hp_X]/mL SUS SCROFA STOMACH;
  • 3 [hp_X]/mL SYZYGIUM CUMINI SEED;
  • 8 [hp_X]/mL WATER


Administration Route(s): ORAL

Dosage Form(s): LIQUID

Pharmacy Class(es):
  • Allergens [CS];
  • Allergens [CS];
  • Calculi Dissolution Agent [EPC];
  • Cell-mediated Immunity [PE];
  • Cell-mediated Immunity [PE];
  • Dietary Proteins [CS];
  • Food Additives [CS];
  • Increased Histamine Release [PE];
  • Increased Histamine Release [PE];
  • Increased Large Intestinal Motility [PE];
  • Increased Large Intestinal Motility [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Large Intestine Fluid/Electrolyte Absorption [PE];
  • Inhibition Small Intestine Fluid/Electrolyte Absorption [PE];
  • Magnesium Ion Exchange Activity [MoA];
  • Magnetic Resonance Contrast Activity [MoA];
  • Non-Standardized Food Allergenic Extract [EPC];
  • Osmotic Activity [MoA];
  • Osmotic Activity [MoA];
  • Osmotic Laxative [EPC];
  • Osmotic Laxative [EPC];
  • Paramagnetic Contrast Agent [EPC];
  • Potassium Compounds [CS];
  • Potassium Salt [EPC];
  • Standardized Chemical Allergen [EPC];
  • Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Labeler Name: Deseret Biologicals, Inc.
Product Type: HUMAN OTC DRUG
FDA Application Number:
Marketing Category: UNAPPROVED HOMEOPATHIC
Start Marketing Date:5/13/2019
End Marketing Date:5/30/2024

Package Information

No. Package Code Package Description Billing Unit
143742-1479-160 mL in 1 BOTTLE, DROPPER (43742-1479-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1479The 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.
PRODUCT TYPE NAMEHUMAN OTC DRUGIndicates 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.
PROPRIETARY NAMEGI DrainageThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMECinnamomum, Gentiana Lutea, Syzygium Jambolanum, Argentum Nitricum, Colchicum Autumnale, Colostrum, Copper Gluconate, Lappa Major, Lycopodium Clavatum, Magnesium Gluconate, Manganese Gluconate, Potassium Gluconate, Rumex Crispus, Scrophularia Nodosa, Stomach (Suis), Aurum Metallicum, Calcarea Carbonica, Carbo Vegetabilis, Intestine (Suis), Malus Pumila, Flos, Nitricum Acidum, Prunus Cerasifera, Flos, Rock Water, Fagus Sylvatica, FlosThe non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAMELIQUIDThe translation of the dosage form Code submitted by the firm.
ROUTE NAMEORALThe translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE5/13/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
END MARKETING DATE5/30/2024This 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.
MARKETING CATEGORY NAMEUNAPPROVED HOMEOPATHICProduct 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.
LABELER NAMEDeseret Biologicals, Inc.Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAMEACTIVATED CHARCOAL; ARCTIUM LAPPA ROOT; BOS TAURUS COLOSTRUM; CINNAMON; COLCHICUM AUTUMNALE BULB; COPPER GLUCONATE; FAGUS SYLVATICA FLOWERING TOP; GENTIANA LUTEA ROOT; GOLD; LYCOPODIUM CLAVATUM SPORE; MAGNESIUM GLUCONATE; MALUS PUMILA FLOWER; MANGANESE GLUCONATE; NITRIC ACID; OYSTER SHELL CALCIUM CARBONATE, CRUDE; PORK INTESTINE; POTASSIUM GLUCONATE; PRUNUS CERASIFERA FLOWER; RUMEX CRISPUS ROOT; SCROPHULARIA NODOSA; SILVER NITRATE; SUS SCROFA STOMACH; SYZYGIUM CUMINI SEED; WATERAn 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.
ACTIVE NUMERATOR STRENGTH8; 6; 6; 3; 6; 6; 12; 3; 8; 6; 6; 8; 6; 8; 8; 8; 6; 8; 6; 6; 6; 6; 3; 8 
ACTIVE INGRED UNIT[hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL 
PHARM CLASSESAllergens [CS], Allergens [CS], Calculi Dissolution Agent [EPC], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Dietary Proteins [CS], Food Additives [CS], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] 

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This page was last updated on: 2/1/2023