44911-0724 NDC - TRACE MINERAL CORD (ARGENTUM METALLICUM, AURUM METALLICUM, BORON CITRATE, CALCAREA FLUORICA, CALCAREA PHOSPHORICA, CALCAREA SULPHURICA, CHROMIUM SULPHURICUM, COBALT GLUCONATE, CUPRUM SULPHURICUM, FERRUM PHOSPHORICUM, GERMANIUM SESQUIOXIDE, IODIUM, KALI BROMATUM, KALI MURIATICUM, KALI PHOSPHORICUM, KALI SULPHURICUM, LITHIUM CARBONICUM, MAGNESIA PHOSPHORICA, MANGANUM MURIATICUM, NATRUM MURIATICUM, NATRUM PHOSPHORICUM, NATRUM SULPHURICUM, SELENIUM METALLICUM, SILICEA, SODIUM MOLYBDATE, STRONTIUM CARBONICUM, VANADIUM METALLICUM,)

Drug Information

Product NDC: 44911-0724
Proprietary Name: Trace Mineral Cord
Non Proprietary Name: Argentum Metallicum, Aurum Metallicum, Boron Citrate, Calcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Chromium Sulphuricum, Cobalt Gluconate, Cuprum Sulphuricum, Ferrum Phosphoricum, Germanium Sesquioxide, Iodium, Kali Bromatum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Lithium Carbonicum, Magnesia Phosphorica, Manganum Muriaticum, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Selenium Metallicum, Silicea, Sodium Molybdate, Strontium Carbonicum, Vanadium Metallicum,
Active Ingredient(s): 8 [hp_X]/mL BORON CITRATE; 8 [hp_X]/mL CALCIUM FLUORIDE; 8 [hp_X]/mL CALCIUM SULFATE ANHYDROUS; 8 [hp_X]/mL CHROMIC SULFATE PENTADECAHYDRATE; 8 [hp_X]/mL COBALTOUS GLUCONATE; 8 [hp_X]/mL CUPRIC SULFATE; 8 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE; 8 [hp_X]/mL FERROSOFERRIC PHOSPHATE; 8 [hp_X]/mL GERMANIUM SESQUIOXIDE; 8 [hp_X]/mL GOLD; 30 [hp_X]/mL INDIUM; 8 [hp_X]/mL IODINE; 8 [hp_X]/mL LITHIUM CARBONATE; 8 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; 8 [hp_X]/mL MANGANESE CHLORIDE; 30 [hp_X]/mL PALLADIUM; 30 [hp_X]/mL PLATINUM; 8 [hp_X]/mL POTASSIUM BROMIDE; 8 [hp_X]/mL POTASSIUM CHLORIDE; 8 [hp_X]/mL POTASSIUM SULFATE; 8 [hp_X]/mL SELENIUM; 8 [hp_X]/mL SILICON DIOXIDE; 8 [hp_X]/mL SILVER; 8 [hp_X]/mL SODIUM CHLORIDE; 8 [hp_X]/mL SODIUM MOLYBDATE; 8 [hp_X]/mL SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; 8 [hp_X]/mL SODIUM SULFATE; 8 [hp_X]/mL STRONTIUM CARBONATE; 8 [hp_X]/mL TRIBASIC CALCIUM PHOSPHATE; 8 [hp_X]/mL VANADIUM; 8 [hp_X]/mL ZINC GLUCONATE
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Allergens [CS]; Blood Coagulation Factor [EPC]; Blood Coagulation Factor [EPC]; Calcium [CS]; Calcium [CS]; Calculi Dissolution Agent [EPC]; Cations; Divalent [CS]; Cations; Divalent [CS]; Cell-mediated Immunity [PE]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Increased Coagulation Factor Activity [PE]; Increased Coagulation Factor Activity [PE]; Increased Histamine Release [PE]; Increased Large Intestinal Motility [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 Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Magnetic Resonance Contrast Activity [MoA]; Mood Stabilizer [EPC]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Osmotic Laxative [EPC]; Paramagnetic Contrast Agent [EPC]; Phosphate Binder [EPC]; Phosphate Binder [EPC]; Phosphate Chelating Activity [MoA]; Phosphate Chelating Activity [MoA]; Potassium Compounds [CS]; Potassium Compounds [CS]; Potassium Salt [EPC]; Potassium Salt [EPC]; Standardized Chemical Allergen [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Field Name	Field Value
Labeler Name:	Energique, Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	12/20/2024

Package Information

No.	Package Code	Package Description	Billing Unit
1	44911-0724-1	59 mL in 1 BOTTLE, DROPPER (44911-0724-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	44911-0724	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.
PRODUCT TYPE NAME	HUMAN OTC DRUG	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.
PROPRIETARY NAME	Trace Mineral Cord	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	Argentum Metallicum, Aurum Metallicum, Boron Citrate, Calcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Chromium Sulphuricum, Cobalt Gluconate, Cuprum Sulphuricum, Ferrum Phosphoricum, Germanium Sesquioxide, Iodium, Kali Bromatum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Lithium Carbonicum, Magnesia Phosphorica, Manganum Muriaticum, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Selenium Metallicum, Silicea, Sodium Molybdate, Strontium Carbonicum, Vanadium Metallicum,	The non-proprietary name is sometimes called the generic name. The generic name usually includes the active ingredient(s) of the product.
DOSAGE FORM NAME	LIQUID	The translation of the dosage form Code submitted by the firm.
ROUTE NAME	ORAL	The translation of the route code submitted by the firm, indicating route of administration.
START MARKETING DATE	12/20/2024	This is the date that the labeler indicates was the start of its marketing of the drug product.
MARKETING CATEGORY NAME	UNAPPROVED HOMEOPATHIC	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.
LABELER NAME	Energique, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	BORON CITRATE; CALCIUM FLUORIDE; CALCIUM SULFATE ANHYDROUS; CHROMIC SULFATE PENTADECAHYDRATE; COBALTOUS GLUCONATE; CUPRIC SULFATE; DIBASIC POTASSIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; GERMANIUM SESQUIOXIDE; GOLD; INDIUM; IODINE; LITHIUM CARBONATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE CHLORIDE; PALLADIUM; PLATINUM; POTASSIUM BROMIDE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SELENIUM; SILICON DIOXIDE; SILVER; SODIUM CHLORIDE; SODIUM MOLYBDATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; STRONTIUM CARBONATE; TRIBASIC CALCIUM PHOSPHATE; VANADIUM; ZINC GLUCONATE	An 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 STRENGTH	8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 30; 8; 8; 8; 8; 30; 30; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
PHARM CLASSES	Allergens [CS], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagulation Factor Activity [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [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 Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Mood Stabilizer [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Drug Information

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