Product NDC: | 50114-1136 |
Proprietary Name: | Tonico-Heel |
Non Proprietary Name: | STRYCHNOS NUX-VOMICA SEED and POTASSIUM PHOSPHATE, DIBASIC and GOLD and QUININE ARSENITE and CHAMAELIRIUM LUTEUM ROOT and HYPERICUM PERFORATUM and SELENIUM |
Active Ingredient(s): | 10; 10; 10; 10; 10; 10; 10 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp; STRYCHNOS NUX-VOMICA SEED and POTASSIUM PHOSPHATE, DIBASIC and GOLD and QUININE ARSENITE and CHAMAELIRIUM LUTEUM ROOT and HYPERICUM PERFORATUM and SELENIUM |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-1136 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 20030831 |
Package NDC: | 50114-1136-2 |
Package Description: | 30000 mg in 1 BOTTLE (50114-1136-2) |
NDC Code | 50114-1136-2 |
Proprietary Name | Tonico-Heel |
Package Description | 30000 mg in 1 BOTTLE (50114-1136-2) |
Product NDC | 50114-1136 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | STRYCHNOS NUX-VOMICA SEED and POTASSIUM PHOSPHATE, DIBASIC and GOLD and QUININE ARSENITE and CHAMAELIRIUM LUTEUM ROOT and HYPERICUM PERFORATUM and SELENIUM |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 20030831 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | CHAMAELIRIUM LUTEUM ROOT; GOLD; HYPERICUM PERFORATUM; POTASSIUM PHOSPHATE, DIBASIC; QUININE ARSENITE; SELENIUM; STRYCHNOS NUX-VOMICA SEED |
Strength Number | 10; 10; 10; 10; 10; 10; 10 |
Strength Unit | [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg |
Pharmaceutical Classes |