Ultra (Soza Clinic)
Welcome to the PulseAid listing for the Ultra drug offered from Soza Clinic. This Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] pharmaceutical is classified as a HUMAN PRESCRIPTION DRUG. Below, you can view details for this drug, such as its dosage form, route of delivery, start market/end market dates, and more. We have also randomly listed additional pharmaceuticals used in the same HUMAN PRESCRIPTION DRUG drug type category.
| LABELER NAME / MANUFACTURER: | Soza Clinic |
| NON-PROPRIETARY NAME: | Ambrosia artemisiaefolia, Anacardium orientale, Baryta muriatica, Calcarea carbonica, Calcarea phosphorica, Fucus Vesiculosus, Helleborus niger, Hypothalamus, Ignatia amara, Lycopodium clavatum, Magne |
| SUBSTANCE NAME: | AMBROSIA ARTEMISIIFOLIA; SEMECARPUS ANACARDIUM JUICE; BARIUM CHLORIDE DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; FUCUS VESICULOSUS; HELLEBORUS NIGER ROOT; BOS TAURUS |
| TYPE: | HUMAN PRESCRIPTION DRUG |
| PHARMA CLASS: | Blood Coagulation Factor [EPC],Increased Coagulation Factor Activity [PE],Calcium [Chemical/Ingredient],Cations, Divalent [Chemical/Ingredient],Calculi Dissolution Agent [EPC],Magnesium Ion Exchange Activity [MoA],Osmotic Laxative [EPC],Osmotic Activity [MoA],Inhibition Small Intestine Fluid/Electrolyte Absorption [PE],Increased Large Intestinal Motility [PE],Stimulation Large Intestine Fluid/Electrolyte Secretion [PE],Inhibition Large Intestine Fluid/Electrolyte Absorption [PE] |
| ROUTE: | ORAL |
| DOSAGE FORM: | LIQUID |
| MARKETING CATEGORY NAME: | UNAPPROVED HOMEOPATHIC |
| START MARKETING DATE: | 2013-05-03 |
| END MARKETING DATE: | 0000-00-00 |
Ultra HUMAN PRESCRIPTION DRUG Details:
| Item Description | Ultra from Soza Clinic |
| LABELER NAME: | Soza Clinic |
| DEA SCHEDULE: |
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| ACTIVE STRENGTH: | 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 10; 12; 12; 12([hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X]/29.6mL; [hp_X) |
| START MARKETING DATE: | 2013-05-03 |
| END MARKETING DATE: | 0000-00-00 |
| PRODUCT ID: | 55924-0001_785dc00b-da8c-415c-908f-a7ee6b23997c |
| PRODUCT NDC: | 55924-0001 |
| APPLICATION NUMBER: | |
Other AMBROSIA ARTEMISIIFOLIA; SEMECARPUS ANACARDIUM JUICE; BARIUM CHLORIDE DIHYDRATE; OYSTER SHELL CALCIUM CARBONATE, CRUDE; TRIBASIC CALCIUM PHOSPHATE; FUCUS VESICULOSUS; HELLEBORUS NIGER ROOT; BOS TAURUS Pharmaceutical Manufacturers / Labelers:
