NDC Code | 17089-299-18 |
Package Description | 1 BOTTLE, DROPPER in 1 BOX (17089-299-18) > 30 mL in 1 BOTTLE, DROPPER |
Product NDC | 17089-299 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Guna-allergy-prev |
Non-Proprietary Name | Ambrosia Artemisiifolia - Anguilla Rostrata Blood Serum - Arundo Pliniana Root - Black Currant - Chelidonium Majus - Citric Acid Monohydrate - Histamine Dihydrochloride - Human Interleukin 12 - Interferon Gamma-1b - Manganese Gluconate - Parietaria Officinalis - Phleum Pratense - Sodium Pyruvate - Sodium Sulfate - Succinic Acid - Sulfur - Urtica Urens - Viburnum Opulus Root - Wyethia Helenioides Root - |
Dosage Form | SOLUTION/ DROPS |
Usage | ORAL |
Start Marketing Date | 20060523 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Manufacturer | Guna spa |
Substance Name | AMBROSIA ARTEMISIIFOLIA; ANGUILLA ROSTRATA BLOOD SERUM; ARUNDO PLINIANA ROOT; ASCLEPIAS CURASSAVICA; BLACK CURRANT; CITRIC ACID MONOHYDRATE; HISTAMINE DIHYDROCHLORIDE; HUMAN INTERLEUKIN 12; INTERFERON GAMMA-1B; MANGANESE GLUCONATE; PARIETARIA OFFICINALIS; PHLEUM PRATENSE; SODIUM PYRUVATE; SODIUM SULFATE; SUCCINIC ACID; SULFUR; URTICA URENS; VIBURNUM OPULUS ROOT; WYETHIA HELENIOIDES ROOT |
Strength | 18; 200; 18; 6; 1; 6; 30; 4; 4; 4; 18; 18; 6; 200; 6; 30; 18; 3; 18 |
Strength Unit | [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; g/30mL; [hp_X]/30mL |
Pharmacy Classes | Acidifying Activity [MoA], Anti-coagulant [EPC], Calcium Chelating Activity [MoA], Calculi Dissolution Agent [EPC], Decreased Coagulation Factor Activity [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Interferon gamma [EPC], Interferon-gamma [CS], Magnetic Resonance Contrast Activity [MoA], Osmotic Activity [MoA], Osmotic Laxative [EPC], Paramagnetic Contrast Agent [EPC] |