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Cardioforce II
Cardioforce II - 57520-0049-1 - (Cardioforce II)
Drug Information of Cardioforce II
| Product NDC: | 57520-0049 |
| Proprietary Name: | Cardioforce II |
| Non Proprietary Name: | Cardioforce II |
| Active Ingredient(s): | 3; 3; 3; 3; 5; 8; 3; 3; 12; 3 [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 & nbsp; Cardioforce II |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
Labeler Information of Cardioforce II
| Product NDC: | 57520-0049 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100208 |
Package Information of Cardioforce II
| Package NDC: | 57520-0049-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0049-1) |
NDC Information of Cardioforce II
| NDC Code | 57520-0049-1 |
| Proprietary Name | Cardioforce II |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0049-1) |
| Product NDC | 57520-0049 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cardioforce II |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100208 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ARTEMISIA ABROTANUM FLOWERING TOP; BLACK COHOSH; CHELIDONIUM MAJUS; CONVALLARIA MAJALIS; MAGNESIUM SULFATE HEPTAHYDRATE; NERIUM OLEANDER LEAF; PEUMUS BOLDUS LEAF; POTASSIUM PHOSPHATE, DIBASIC; SODIUM CHLORIDE; TARAXACUM OFFICINALE |
| Strength Number | 3; 3; 3; 3; 5; 8; 3; 3; 12; 3 |
| 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 |
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