Product NDC: | 50114-6090 |
Proprietary Name: | Lithiumeel |
Non Proprietary Name: | STRYCHNOS NUX-VOMICA SEED and TOXICODENDRON PUBESCENS LEAF and LITHIUM CARBONATE and COLCHICUM AUTUMNALE BULB and SODIUM CARBONATE and FERROSOFERRIC PHOSPHATE |
Active Ingredient(s): | 4; 6; 3; 4; 6; 6 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp; STRYCHNOS NUX-VOMICA SEED and TOXICODENDRON PUBESCENS LEAF and LITHIUM CARBONATE and COLCHICUM AUTUMNALE BULB and SODIUM CARBONATE and FERROSOFERRIC PHOSPHATE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-6090 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19840131 |
Package NDC: | 50114-6090-2 |
Package Description: | 30000 mg in 1 BOTTLE (50114-6090-2) |
NDC Code | 50114-6090-2 |
Proprietary Name | Lithiumeel |
Package Description | 30000 mg in 1 BOTTLE (50114-6090-2) |
Product NDC | 50114-6090 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | STRYCHNOS NUX-VOMICA SEED and TOXICODENDRON PUBESCENS LEAF and LITHIUM CARBONATE and COLCHICUM AUTUMNALE BULB and SODIUM CARBONATE and FERROSOFERRIC PHOSPHATE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19840131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | COLCHICUM AUTUMNALE BULB; FERROSOFERRIC PHOSPHATE; LITHIUM CARBONATE; SODIUM CARBONATE; STRYCHNOS NUX-VOMICA SEED; TOXICODENDRON PUBESCENS LEAF |
Strength Number | 4; 6; 3; 4; 6; 6 |
Strength Unit | [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg |
Pharmaceutical Classes |