NDC Code | 44911-0437-1 |
Package Description | 30 mL in 1 BOTTLE, DROPPER (44911-0437-1) |
Product NDC | 44911-0437 |
Product Type Name | HUMAN OTC DRUG |
Proprietary Name | Fungustat |
Proprietary Name Suffix | Ii |
Non-Proprietary Name | Echinacea (angustifolia), Fucus Vesiculosus, Hydrastis Canadensis, Phytolacca Decandra, Kreosotum, Natrum Muriaticum, Candida Albicans, Lycopodium Clavatum, Pulsatilla (pratensis), Sepia |
Dosage Form | LIQUID |
Usage | ORAL |
Start Marketing Date | 20170905 |
End Marketing Date | 20250413 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Manufacturer | Energique, Inc. |
Substance Name | ANEMONE PRATENSIS; CANDIDA ALBICANS; ECHINACEA ANGUSTIFOLIA; FUCUS VESICULOSUS; GOLDENSEAL; LYCOPODIUM CLAVATUM SPORE; PHYTOLACCA AMERICANA ROOT; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE; WOOD CREOSOTE |
Strength | 30; 12; 3; 3; 6; 30; 6; 30; 12; 12 |
Strength Unit | [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 |
Pharmacy Classes | Allergens [CS], Cell-mediated Immunity [PE], Fungal Proteins [CS], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Fungal Allergenic Extract [EPC] |