Free Radical
- Product NDC
- 43742-1289
- 11-digit product format
- 437421289
- Labeler code
- 43742
- Product ID
- 43742-1289_2f620e4a-9896-45e4-881f-bd88816e6687
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Alfalfa, Ascorbyl Palmitate, Cysteinum, Hordeum Vulgare, Laminaria Digitata, Manganese Gluconate, L-Methionine, Nasturtium Aquaticum, Dimethyl Glycine, Quercetin, Raphanus Sativus, Sodium Selenite, Triticum Aestivum, Ubidecarenonum, GABA (Gamma Aminobutyric Acid), alpha-Lipoicum Acidum, Oryza Sativa, Tocopherol, Zinc Picolinate, Cobaltum Metallicum, Ferrum Metallicum, Glutathione, Magnesium Fluoratum, Selenium Metallicum, Zincum Metallicum, alpha-Ketoglutaricum Acidum, Glyoxal Trimer Dihydrate
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2018-11-30
- Marketing end
- 2024-02-01
- Substance
- .ALPHA.-KETOGLUTARIC ACID; .ALPHA.-LIPOIC ACID; .GAMMA.-AMINOBUTYRIC ACID; ALFALFA; ASCORBYL PALMITATE; BARLEY; COBALT; CYSTEINE; GLUTATHIONE; GLYOXAL TRIMER DIHYDRATE; IRON; LAMINARIA DIGITATA; MAGNESIUM FLUORIDE; MANGANESE GLUCONATE; METHIONINE; N,N-DIMETHYLGLYCINE; NASTURTIUM OFFICINALE; ORYZA SATIVA WHOLE; QUERCETIN; RAPHANUS SATIVUS; SELENIUM; SODIUM SELENITE; TOCOPHEROL; UBIDECARENONE; WHEAT; ZINC; ZINC PICOLINATE
- Active strength
- 30 [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
- Listing certified through
- 0000-00-00
- Current FDA listing
- Historical FDA.report record
Packages#
Package NDC, 11-digit format, Description table| Package NDC | 11-digit format | Description | Units | Marketing start | Marketing end | Sample | Exclude flag | Status |
|---|
| 43742-1289-1 | 43742128901 | 30 mL in 1 BOTTLE, DROPPER (43742-1289-1) | 30 ml | 2018-11-30 | 0000-00-00 | No | No | Current |