43742-2247 NDC - EMF PROTECT AND BALANCE (ALFALFA, CADMIUM SULPHURATUM, CALCAREA CARBONICA, CUPRUM METALLICUM, FERRUM METALLICUM, FUCUS VESICULOSUS, HYPERICUM PERFORATUM, KALI PHOSPHORICUM, MAGNESIA PHOSPHORICA, MANGANUM METALLICUM, MERCURIUS VIVUS, PLUMBUM METALLICUM, SILICEA, SYMPHYTUM OFFICINALE, TARENTULA HISPANA, X-RAY, YTTERBIUM OXIDE)

Drug Information

Product NDC: 43742-2247
Proprietary Name: EMF Protect and Balance
Non Proprietary Name: Alfalfa, Cadmium Sulphuratum, Calcarea Carbonica, Cuprum Metallicum, Ferrum Metallicum, Fucus Vesiculosus, Hypericum Perforatum, Kali Phosphoricum, Magnesia Phosphorica, Manganum Metallicum, Mercurius Vivus, Plumbum Metallicum, Silicea, Symphytum Officinale, Tarentula Hispana, X-Ray, Ytterbium Oxide
Active Ingredient(s): 20 [hp_X]/mL ALCOHOL, X-RAY EXPOSED (1000 RAD); 12 [hp_X]/mL CADMIUM SULFIDE; 6 [hp_X]/mL COMFREY ROOT; 30 [hp_X]/mL COPPER; 3 [hp_X]/mL DIBASIC POTASSIUM PHOSPHATE; 3 [hp_X]/mL FUCUS VESICULOSUS; 12 [hp_X]/mL HYPERICUM PERFORATUM WHOLE; 8 [hp_X]/mL IRON; 12 [hp_X]/mL LEAD; 16 [hp_X]/mL LYCOSA TARANTULA; 12 [hp_X]/mL MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; 12 [hp_X]/mL MANGANESE; 3 [hp_X]/mL MEDICAGO SATIVA WHOLE; 12 [hp_X]/mL MERCURY; 8 [hp_X]/mL OYSTER SHELL CALCIUM CARBONATE, CRUDE; 30 [hp_X]/mL SILICON DIOXIDE; 12 [hp_X]/mL YTTERBIUM OXIDE
Administration Route(s): ORAL
Dosage Form(s): LIQUID
Pharmacy Class(es): Calculi Dissolution Agent [EPC]; Copper [CS]; Copper-containing Intrauterine Device [EPC]; Decreased Embryonic Implantation [PE]; Decreased Sperm Motility [PE]; Increased Large Intestinal Motility [PE]; Inhibit Ovum Fertilization [PE]; Inhibition Large Intestine Fluid/Electrolyte Absorption [PE]; Inhibition Small Intestine Fluid/Electrolyte Absorption [PE]; Magnesium Ion Exchange Activity [MoA]; Osmotic Activity [MoA]; Osmotic Laxative [EPC]; Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Labeler Information

Field Name	Field Value
Labeler Name:	Deseret Biologicals, Inc.
Product Type:	HUMAN OTC DRUG
FDA Application Number:
Marketing Category:	UNAPPROVED HOMEOPATHIC
Start Marketing Date:	3/17/2025

Package Information

No.	Package Code	Package Description	Billing Unit
1	43742-2247-1	30 mL in 1 BOTTLE, DROPPER (43742-2247-1)

NDC Record

Field Name	Field Value	Definition
PRODUCT NDC	43742-2247	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	EMF Protect and Balance	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	Alfalfa, Cadmium Sulphuratum, Calcarea Carbonica, Cuprum Metallicum, Ferrum Metallicum, Fucus Vesiculosus, Hypericum Perforatum, Kali Phosphoricum, Magnesia Phosphorica, Manganum Metallicum, Mercurius Vivus, Plumbum Metallicum, Silicea, Symphytum Officinale, Tarentula Hispana, X-Ray, Ytterbium Oxide	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	3/17/2025	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	Deseret Biologicals, Inc.	Name of Company corresponding to the labeler code segment of the Product NDC.
SUBSTANCE NAME	ALCOHOL, X-RAY EXPOSED (1000 RAD); CADMIUM SULFIDE; COMFREY ROOT; COPPER; DIBASIC POTASSIUM PHOSPHATE; FUCUS VESICULOSUS; HYPERICUM PERFORATUM WHOLE; IRON; LEAD; LYCOSA TARANTULA; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE; MEDICAGO SATIVA WHOLE; MERCURY; OYSTER SHELL CALCIUM CARBONATE, CRUDE; SILICON DIOXIDE; YTTERBIUM OXIDE	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	20; 12; 6; 30; 3; 3; 12; 8; 12; 16; 12; 12; 3; 12; 8; 30; 12
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
PHARM CLASSES	Calculi Dissolution Agent [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]

Drug Information

Labeler Information

Package Information

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