Product ID | 44911-0335_1148fa93-c689-48b4-93d5-c07ee221468c |
NDC | 44911-0335 |
Product Type | Human Otc Drug |
Proprietary Name | Scrophularitone |
Generic Name | Baptisia Tinctoria, Echinacea (angustifolia), Trifolium Pratense, Phytolacca Decandra, Arsenicum Iodatum, Baryta Carbonica, Bromium, Calcarea Carbonica, Kali Muriaticum, Lachesis Mutus, Mercurius Solubilis |
Dosage Form | Liquid |
Route of Administration | ORAL |
Marketing Start Date | 2016-03-30 |
Marketing End Date | 2024-10-24 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Energique, Inc. |
Substance Name | ARSENIC TRIIODIDE; BAPTISIA TINCTORIA ROOT; BARIUM CARBONATE; BROMINE; ECHINACEA ANGUSTIFOLIA; LACHESIS MUTA VENOM; MERCURIUS SOLUBILIS; PHYTOLACCA AMERICANA ROOT; POTASSIUM CHLORIDE; TRIFOLIUM PRATENSE FLOWER |
Active Ingredient Strength | 12 [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 |
Pharm Classes | Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA], Osmotic Laxative [EPC], Potassium Compounds [CS], Potassium Salt [EPC] |
NDC Exclude Flag | N |