NDC Code | 48951-9177-1 |
Package Description | 10 AMPULE in 1 BOX (48951-9177-1) > 1 mL in 1 AMPULE |
Product NDC | 48951-9177 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Urtica Betula Special Order |
Non-Proprietary Name | Urtica Betula Special Order |
Dosage Form | LIQUID |
Usage | ORAL |
Start Marketing Date | 20090901 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Manufacturer | Uriel Pharmacy Inc. |
Substance Name | BETULA PUBESCENS LEAF; BOS TAURUS BONE MARROW; FERROSOFERRIC PHOSPHATE; MAGNESIUM PHOSPHATE, TRIBASIC, PENTAHYDRATE; SILVER SULFIDE; URTICA DIOICA |
Strength | 4; 8; 6; 6; 6; 3 |
Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
Pharmacy Classes | Calculi Dissolution Agent [EPC], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Inhibition Small Intestine Fluid/Electrolyte Absorption [PE], Magnesium Ion Exchange Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Stimulation Large Intestine Fluid/Electrolyte Secretion [PE] |