| Product NDC: | 57520-0058 |
| Proprietary Name: | Energize |
| Non Proprietary Name: | Energize |
| Active Ingredient(s): | 6; 3; 3; 6; 12; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Energize |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57520-0058 |
| Labeler Name: | Apothica Company |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100125 |
| Package NDC: | 57520-0058-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0058-1) |
| NDC Code | 57520-0058-1 |
| Proprietary Name | Energize |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0058-1) |
| Product NDC | 57520-0058 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | Energize |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100125 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apothica Company |
| Substance Name | AMERICAN GINSENG; AVENA SATIVA FLOWERING TOP; GINGER; PHOSPHORIC ACID; POTASSIUM PHOSPHATE, DIBASIC; TRINITROPHENOL |
| Strength Number | 6; 3; 3; 6; 12; 6 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes | Non-Standardized Plant Allergenic Extract [EPC],Non-Standardized Food Allergenic Extract [EPC],Increased Histamine Release [PE],Cell-mediated Immunity [PE],Allergens [Chemical/Ingredient],Dietary Proteins [Chemical/Ingredient],Plant Proteins [Chemical/Ingredient],Food Additives [Chemical/Ingredient],Potassium Compounds [Chemical/Ingredient],Potassium Salt [EPC] |