43742-1561 NDC - FREE RADICAL (ALFALFA, ASCORBYL PALMITATE, CYSTEINUM, DIMETHYL GLYCINE, FUCUS VESICULOSUS, HORDEUM VULGARE, L-METHIONINE, MANGANESE GLUCONATE, NASTURTIUM AQUATICUM, QUERCETIN, RAPHANUS SATIVUS, SODIUM SELENITE, TRITICUM AESTIVUM, UBIDECARENONUM, ALPHA-LIPOICUM ACIDUM, GABA (GAMMA AMINOBUTYRIC ACID), ORYZA SATIVA, VITAMIN E, ZINC PICOLINATE, COBALTUM METALLICUM, FERRUM METALLICUM, GLUTATHIONE, MAGNESIUM FLUORATUM, SELENIUM METALLICUM, ZINCUM METALLICUM, ALPHA-KETOGLUTARICUM ACIDUM)

Drug Information

  • Product NDC: 43742-1561
  • Proprietary Name: Free Radical
  • Non Proprietary Name: Alfalfa, Ascorbyl Palmitate, Cysteinum, Dimethyl Glycine, Fucus Vesiculosus, Hordeum Vulgare, L-Methionine, Manganese Gluconate, Nasturtium Aquaticum, Quercetin, Raphanus Sativus, Sodium Selenite, Triticum Aestivum, Ubidecarenonum, alpha-Lipoicum Acidum, GABA (Gamma Aminobutyric Acid), Oryza Sativa, Vitamin E, Zinc Picolinate, Cobaltum Metallicum, Ferrum Metallicum, Glutathione, Magnesium Fluoratum, Selenium Metallicum, Zincum Metallicum, alpha-Ketoglutaricum Acidum
  • Active Ingredient(s): 30 [hp_X]/mL .ALPHA.-KETOGLUTARIC ACID; 8 [hp_X]/mL .ALPHA.-LIPOIC ACID; 8 [hp_X]/mL .ALPHA.-TOCOPHEROL; 8 [hp_X]/mL .GAMMA.-AMINOBUTYRIC ACID; 30 [hp_X]/mL ACETALDEHYDE; 6 [hp_X]/mL ASCORBYL PALMITATE; 6 [hp_X]/mL BARLEY; 12 [hp_X]/mL COBALT; 6 [hp_X]/mL CYSTEINE; 6 [hp_X]/mL FUCUS VESICULOSUS; 12 [hp_X]/mL GLUTATHIONE; 12 [hp_X]/mL IRON; 12 [hp_X]/mL MAGNESIUM FLUORIDE; 6 [hp_X]/mL MANGANESE GLUCONATE; 6 [hp_X]/mL MEDICAGO SATIVA WHOLE; 6 [hp_X]/mL METHIONINE; 6 [hp_X]/mL N,N-DIMETHYLGLYCINE; 6 [hp_X]/mL NASTURTIUM OFFICINALE; 8 [hp_X]/mL ORYZA SATIVA WHOLE; 6 [hp_X]/mL QUERCETIN; 6 [hp_X]/mL RAPHANUS SATIVUS; 12 [hp_X]/mL SELENIUM; 6 [hp_X]/mL SODIUM SELENITE; 6 [hp_X]/mL UBIDECARENONE; 6 [hp_X]/mL WHEAT; 12 [hp_X]/mL ZINC; 8 [hp_X]/mL ZINC PICOLINATE
  • Administration Route(s): ORAL
  • Dosage Form(s): LIQUID
  • Pharmacy Class(es): Allergens [CS]; Allergens [CS]; Allergens [CS]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Cell-mediated Immunity [PE]; Copper Absorption Inhibitor [EPC]; Decreased Copper Ion Absorption [PE]; Dietary Proteins [CS]; Dietary Proteins [CS]; Grain Proteins [EXT]; Grain Proteins [EXT]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Increased Histamine Release [PE]; Magnetic Resonance Contrast Activity [MoA]; Non-Standardized Food Allergenic Extract [EPC]; Non-Standardized Food Allergenic Extract [EPC]; Paramagnetic Contrast Agent [EPC]; Standardized Chemical Allergen [EPC]

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:9/6/2019

Package Information

No. Package Code Package Description Billing Unit
143742-1561-130 mL in 1 BOTTLE, DROPPER (43742-1561-1)

NDC Record

Field Name Field Value Definition
PRODUCT NDC43742-1561The 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 NAMEFree RadicalThe proprietary name also known as the trade name is the name of the product chosen by the medication labeler for marketing purposes.
NON PROPRIETARY NAMEAlfalfa, Ascorbyl Palmitate, Cysteinum, Dimethyl Glycine, Fucus Vesiculosus, Hordeum Vulgare, L-Methionine, Manganese Gluconate, Nasturtium Aquaticum, Quercetin, Raphanus Sativus, Sodium Selenite, Triticum Aestivum, Ubidecarenonum, alpha-Lipoicum Acidum, GABA (Gamma Aminobutyric Acid), Oryza Sativa, Vitamin E, Zinc Picolinate, Cobaltum Metallicum, Ferrum Metallicum, Glutathione, Magnesium Fluoratum, Selenium Metallicum, Zincum Metallicum, alpha-Ketoglutaricum AcidumThe 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 DATE9/6/2019This is the date that the labeler indicates was the start of its marketing of the drug product.
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 NAME.ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; .ALPHA.-TOCOPHEROL; .GAMMA.-AMINOBUTYRIC ACID; ACETALDEHYDE; ASCORBYL PALMITATE; BARLEY; COBALT; CYSTEINE; FUCUS VESICULOSUS; GLUTATHIONE; IRON; MAGNESIUM FLUORIDE; MANGANESE GLUCONATE; MEDICAGO SATIVA WHOLE; METHIONINE; N,N-DIMETHYLGLYCINE; NASTURTIUM OFFICINALE; ORYZA SATIVA WHOLE; QUERCETIN; RAPHANUS SATIVUS; SELENIUM; SODIUM SELENITE; UBIDECARENONE; WHEAT; ZINC; ZINC PICOLINATEAn 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 STRENGTH30; 8; 8; 8; 30; 6; 6; 12; 6; 6; 12; 12; 12; 6; 6; 6; 6; 6; 8; 6; 6; 12; 6; 6; 6; 12; 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 
PHARM CLASSESAllergens [CS], Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Dietary Proteins [CS], Dietary Proteins [CS], Grain Proteins [EXT], Grain Proteins [EXT], Increased Histamine Release [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Magnetic Resonance Contrast Activity [MoA], Non-Standardized Food Allergenic Extract [EPC], Non-Standardized Food Allergenic Extract [EPC], Paramagnetic Contrast Agent [EPC], Standardized Chemical Allergen [EPC] 

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This page was last updated on: 12/6/2025

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