- Product NDC
- 44911-0724
- 11-digit product format
- 449110724
- Labeler code
- 44911
- Product ID
- 44911-0724_44c3a67d-ce87-4c73-acb6-c3af9315b1aa
- Type
- HUMAN OTC DRUG
- Nonproprietary name
- Argentum Metallicum, Aurum Metallicum, Boron Citrate, Calcarea Fluorica, Calcarea Phosphorica, Calcarea Sulphurica, Chromium Sulphuricum, Cobalt Gluconate, Cuprum Sulphuricum, Ferrum Phosphoricum, Germanium Sesquioxide, Iodium, Kali Bromatum, Kali Muriaticum, Kali Phosphoricum, Kali Sulphuricum, Lithium Carbonicum, Magnesia Phosphorica, Manganum Muriaticum, Natrum Muriaticum, Natrum Phosphoricum, Natrum Sulphuricum, Selenium Metallicum, Silicea, Sodium Molybdate, Strontium Carbonicum, Vanadium Metallicum,
- Dosage form
- LIQUID
- Route
- ORAL
- Labeler
- Energique, Inc.
- Marketing category
- UNAPPROVED HOMEOPATHIC
- Marketing start
- 2024-12-20
- Substance
- BORON CITRATE; CALCIUM FLUORIDE; CALCIUM SULFATE ANHYDROUS; CHROMIC SULFATE PENTADECAHYDRATE; COBALTOUS GLUCONATE; CUPRIC SULFATE; DIBASIC POTASSIUM PHOSPHATE; FERROSOFERRIC PHOSPHATE; GERMANIUM SESQUIOXIDE; GOLD; INDIUM; IODINE; LITHIUM CARBONATE; MAGNESIUM PHOSPHATE, DIBASIC TRIHYDRATE; MANGANESE CHLORIDE; PALLADIUM; PLATINUM; POTASSIUM BROMIDE; POTASSIUM CHLORIDE; POTASSIUM SULFATE; SELENIUM; SILICON DIOXIDE; SILVER; SODIUM CHLORIDE; SODIUM MOLYBDATE; SODIUM PHOSPHATE, DIBASIC, HEPTAHYDRATE; SODIUM SULFATE; STRONTIUM CARBONATE; TRIBASIC CALCIUM PHOSPHATE; VANADIUM; ZINC GLUCONATE
- Active strength
- 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 30; 8; 8; 8; 8; 30; 30; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 8; 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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
- Pharmacologic classes
- Allergens [CS], Blood Coagulation Factor [EPC], Blood Coagulation Factor [EPC], Calcium [CS], Calcium [CS], Calculi Dissolution Agent [EPC], Cations, Divalent [CS], Cations, Divalent [CS], Cell-mediated Immunity [PE], Copper Absorption Inhibitor [EPC], Decreased Copper Ion Absorption [PE], Increased Coagulation Factor Activity [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], 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], Magnesium Ion Exchange Activity [MoA], Magnetic Resonance Contrast Activity [MoA], Mood Stabilizer [EPC], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC], Phosphate Binder [EPC], Phosphate Binder [EPC], Phosphate Chelating Activity [MoA], Phosphate Chelating Activity [MoA], Potassium Compounds [CS], Potassium Compounds [CS], Potassium Salt [EPC], Potassium Salt [EPC], Standardized Chemical Allergen [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE]
- NDC exclude flag
- No
- Listing certified through
- 2026-12-31
- Current FDA listing
- Yes