- Product NDC
- 43742-2082
- 11-digit product format
- 437422082
- Labeler code
- 43742
- Product ID
- 43742-2082_f54b98c8-6033-4765-b9b0-639f0870993f
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Kali Muriaticum, L-Arginine, L-Carnitine, L-Leucine, L-Ornithine, L-Valine, Magnesia Muriatica, Ascorbicum Acidum, Borax, Chromium Oxydatum, Ferrum Muriaticum, Kali Carbonicum, Magnesium Gluconicum Dihydricum, Natrum Muriaticum, Zincum Gluconicum, Cuprum Metallicum, Kali Phosphoricum, Niccolum Metallicum, Selenium Metallicum, Vanadium Metallicum, Calcarea Carbonica, Calcarea Phosphorica, Manganum Carbonicum
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Deseret Biologicals, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2023-10-10
- Substance
- ARGININE; ASCORBIC ACID; CHROMIC OXIDE; COPPER; DIBASIC POTASSIUM PHOSPHATE; FERRIC CHLORIDE HEXAHYDRATE; LEUCINE; LEVOCARNITINE; MAGNESIUM CHLORIDE; MAGNESIUM GLUCONATE; MANGANESE CARBONATE; NICKEL; ORNITHINE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; POTASSIUM CARBONATE; POTASSIUM CHLORIDE; SELENIUM; SODIUM BORATE; SODIUM CHLORIDE; TRIBASIC CALCIUM PHOSPHATE; VALINE; VANADIUM; ZINC GLUCONATE
- Active strength
- 3; 6; 6; 8; 8; 6; 3; 3; 3; 6; 9; 8; 3; 9; 6; 3; 8; 6; 6; 9; 3; 8; 6 [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], Ascorbic Acid [CS], Blood Coagulation Factor [EPC], Calcium [CS], Calculi Dissolution Agent [EPC], Calculi Dissolution Agent [EPC], Carnitine Analog [EPC], Carnitine [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Copper Ion Absorption [PE], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Increased Coagulation Factor Activity [PE], Increased Histamine Release [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Increased Large Intestinal Motility [PE], Inhibit Ovum Fertilization [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Iron [CS], Magnesium Ion Exchange Activity [MoA], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Parenteral Iron Replacement [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE], Vitamin C [EPC]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes