Home NDC 43742-1561 Free Radical
Product NDC 43742-1561
11-digit product format 437421561
Labeler code 43742
Product ID 43742-1561_4a4c582e-202a-46d3-ad52-9127f1752e3c
Type HUMAN OTC DRUG
Nonproprietary 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
Dosage form LIQUID
Route ORAL
Labeler Deseret Biologicals, Inc.
Marketing category UNAPPROVED HOMEOPATHIC
Marketing start 2019-09-06
Marketing end 2029-04-29
Substance .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 PICOLINATE
Active strength 30; 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 [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
Pharmacologic classes 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]
NDC exclude flag No
Current FDA listing Yes Additional Listing Data#
Finished product Yes
Brand name base Free Radical Active Ingredients# Ingredient, Strength table Ingredient Strength MEDICAGO SATIVA WHOLE 30 [hp_X]/mL ASCORBYL PALMITATE 8 [hp_X]/mL CYSTEINE 8 [hp_X]/mL N,N-DIMETHYLGLYCINE 8 [hp_X]/mL FUCUS VESICULOSUS 30 [hp_X]/mL BARLEY 6 [hp_X]/mL METHIONINE 6 [hp_X]/mL MANGANESE GLUCONATE 12 [hp_X]/mL NASTURTIUM OFFICINALE 6 [hp_X]/mL QUERCETIN 6 [hp_X]/mL RAPHANUS SATIVUS 12 [hp_X]/mL SODIUM SELENITE 12 [hp_X]/mL WHEAT 12 [hp_X]/mL UBIDECARENONE 6 [hp_X]/mL .ALPHA.-LIPOIC ACID 6 [hp_X]/mL .GAMMA.-AMINOBUTYRIC ACID 6 [hp_X]/mL ORYZA SATIVA WHOLE 6 [hp_X]/mL .ALPHA.-TOCOPHEROL 6 [hp_X]/mL ZINC PICOLINATE 8 [hp_X]/mL COBALT 6 [hp_X]/mL IRON 6 [hp_X]/mL GLUTATHIONE 12 [hp_X]/mL MAGNESIUM FLUORIDE 6 [hp_X]/mL SELENIUM 6 [hp_X]/mL ZINC 6 [hp_X]/mL ACETALDEHYDE 12 [hp_X]/mL .ALPHA.-KETOGLUTARIC ACID 8 [hp_X]/mL
Harmonized UNII identifiers# UNII identifiers page 1 of 2 · 27 matching rows.
Harmonized SPL set identifiers# SPL set identifiers page 1 of 1 · 1 matching rows.
DailyMed Product Concepts# DailyMed Package Descriptions# Package NDC, Product, Description table Package NDC Product Description Form Quantity Strength SPL version 43742-1561-1 Free Radical 30 mL in 1 BOTTLE, DROPPER LIQUID 30 5
DailyMed Dashboard NDC Coverage# NDC, Dashboard title, SPL version table NDC Dashboard title SPL version Validation Dashboard ZIP 43742-1561 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) LIQUID [DESERET BIOLOGICALS, INC.] 4 Current NDC, Legacy NDC, 1 package rows 20240406_36060680-f0d2-44c3-82fa-649e6e9d454d.zip
openFDA label cross-check# OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.
Matched openFDA labels page 1 of 1 · 1 matching rows.
Brand, Generic, Manufacturer table Brand Generic Manufacturer SPL set ID Effective date Available safety fields Join 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 Deseret Biologicals, Inc. 36060680-f0d2-44c3-82fa-649e6e9d454d 2026-05-06 Warnings Exact identifier ndc (product): 43742-1561
Packages# Package NDC, 11-digit format, Description table Package NDC 11-digit format Description Units Marketing start Marketing end Sample Exclude flag Status 43742-1561-1 43742156101 30 mL in 1 BOTTLE, DROPPER (43742-1561-1) 30 ml 2019-09-06 2029-04-29 No No Current