| Drug NDC: | 43742-1561 |
| 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. | |
| Proprietary Name: | Free Radical |
| Also known as the trade name. It is the name of the product chosen by the labeler. | |
| Product Type: | Human Otc Drug |
| Indicates the type of product, such as Human Prescription Drug or Human OTC Drug. This data element corresponds to the “Document Type” of the SPL submission for the listing. | |
| 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 |
| Also known as the generic name, this is usually the active ingredient(s) of the product. | |
| Labeler Name: | Deseret Biologicals, Inc. |
| Name of Company corresponding to the labeler code segment of the ProductNDC. | |
| Dosage Form: | Liquid |
| The translation of the DosageForm Code submitted by the firm. There is no standard, but values may include terms like `tablet` or `solution for injection`.The complete list of codes and translations can be found www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Status: | Active |
| FDA does not review and approve unfinished products. Therefore, all products in this file are considered unapproved. | |
| Substance Name: | .ALPHA.-KETOGLUTARIC ACID - 30 [hp_X]/mL .ALPHA.-LIPOIC ACID - 8 [hp_X]/mL .ALPHA.-TOCOPHEROL - 8 [hp_X]/mL .GAMMA.-AMINOBUTYRIC ACID - 8 [hp_X]/mL ACETALDEHYDE - 30 [hp_X]/mL ALFALFA - 6 [hp_X]/mL ASCORBYL PALMITATE - 6 [hp_X]/mL BARLEY - 6 [hp_X]/mL COBALT - 12 [hp_X]/mL CYSTEINE - 6 [hp_X]/mL Load more... FUCUS VESICULOSUS - 6 [hp_X]/mL GLUTATHIONE - 12 [hp_X]/mL IRON - 12 [hp_X]/mL MAGNESIUM FLUORIDE - 12 [hp_X]/mL MANGANESE GLUCONATE - 6 [hp_X]/mL METHIONINE - 6 [hp_X]/mL N,N-DIMETHYLGLYCINE - 6 [hp_X]/mL NASTURTIUM OFFICINALE - 6 [hp_X]/mL ORYZA SATIVA WHOLE - 8 [hp_X]/mL QUERCETIN - 6 [hp_X]/mL RAPHANUS SATIVUS - 6 [hp_X]/mL SELENIUM - 12 [hp_X]/mL SODIUM SELENITE - 6 [hp_X]/mL UBIDECARENONE - 6 [hp_X]/mL WHEAT - 6 [hp_X]/mL ZINC - 12 [hp_X]/mL ZINC PICOLINATE - 8 [hp_X]/mL |
| This is the active ingredient list. Each ingredient name is the preferred term of the UNII code submitted. | |
| Route Details: | ORAL |
| The translation of the Route Code submitted by the firm, indicating route of administration. The complete list of codes and translations can be found at www.fda.gov/edrls under Structured Product Labeling Resources. | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Product types are broken down into several potential Marketing Categories, such as New Drug Application (NDA), Abbreviated New Drug Application (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. | |
| Marketing Start Date: | 06 Sep, 2019 |
| This is the date that the labeler indicates was the start of its marketing of the drug product. | |
| Marketing End Date: | 12 Jun, 2026 |
| This 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. | |
| Listing Expiration Date: | 31 Dec, 2024 |
| This is the date when the listing record will expire if not updated or certified by the firm. | |
| Manufacturer Name: | Deseret Biologicals, Inc. |
| Name of manufacturer or company that makes this drug product, corresponding to the labeler code segment of the NDC. | |
| Original Packager: | Yes |
| Whether or not the drug has been repackaged for distribution. | |
| NUI: | N0000185371 N0000175629 N0000184306 M0000728 M0006342 N0000185016 N0000185508 |
| Unique identifier applied to a drug concept within the National Drug File Reference Terminology (NDF-RT). | |
| UNII: | 8ID597Z82X 73Y7P0K73Y H4N855PNZ1 2ACZ6IPC6I GO1N1ZPR3B DJO934BRBD QN83US2B0N 5PWM7YLI7R 3G0H8C9362 K848JZ4886 Load more... 535G2ABX9M GAN16C9B8O E1UOL152H7 5N014C7IWU 9YY2F980SV AE28F7PNPL 7797M4CPPA YH89GMV676 84IVV0906Z 9IKM0I5T1E 86R5J6D01D H6241UJ22B HIW548RQ3W EJ27X76M46 4J2I0SN84Y J41CSQ7QDS ALO92O31SE |
| Unique Ingredient Identifier, which is a non-proprietary, free, unique, unambiguous, non-semantic, alphanumeric identifier based on a substance’s molecular structure and/or descriptive information. | |
| Pharmacologic Class EPC: | Non-Standardized Food Allergenic Extract [EPC] Standardized Chemical Allergen [EPC] |
| Established pharmacologic class associated with an approved indication of an active moiety (generic drug) that the FDA has determined to be scientifically valid and clinically meaningful. Takes the form of the pharmacologic class, followed by `[EPC]` (such as `Thiazide Diuretic [EPC]` or `Tumor Necrosis Factor Blocker [EPC]`. | |
| Pharmacologic Class PE: | Increased Histamine Release [PE] Cell-mediated Immunity [PE] |
| Physiologic effect or pharmacodynamic effect—tissue, organ, or organ system level functional activity—of the drug’s established pharmacologic class. Takes the form of the effect, followed by `[PE]` (such as `Increased Diuresis [PE]` or `Decreased Cytokine Activity [PE]`. | |
| Pharmacologic Class CS: | Allergens [CS] Dietary Proteins [CS] |
| Chemical structure classification of the drug product’s pharmacologic class. Takes the form of the classification, followed by `[Chemical/Ingredient]` (such as `Thiazides [Chemical/Ingredient]` or `Antibodies, Monoclonal [Chemical/Ingredient]. | |
| Pharmacologic Class: | Allergens [CS] Cell-mediated Immunity [PE] Copper Absorption Inhibitor [EPC] Decreased Copper Ion Absorption [PE] Dietary Proteins [CS] Grain Proteins [EXT] Increased Histamine Release [PE] Magnetic Resonance Contrast Activity [MoA] Non-Standardized Food Allergenic Extract [EPC] Paramagnetic Contrast Agent [EPC] Standardized Chemical Allergen [EPC] |
| These are the reported pharmacological class categories corresponding to the SubstanceNames listed above. | |
| Package NDC | Description | Marketing Start Date | Marketing End Date | Sample Available |
|---|---|---|---|---|
| 43742-1561-1 | 30 mL in 1 BOTTLE, DROPPER (43742-1561-1) | 06 Sep, 2019 | N/A | No |
| Package NDC number, known as the NDC, identifies the labeler, product, and trade package size. The first segment, the labeler code, is assigned by the FDA. Description tells the size and type of packaging in sentence form. Multilevel packages will have the descriptions concatenated together. | ||||
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