| Product NDC: | 57520-0512 |
| Proprietary Name: | Pre/Post Surgery |
| Non Proprietary Name: | Hypericum perforatum, Symphytum officinale, Arnica montana |
| Active Ingredient(s): | 200; 12; 12 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL & nbsp; Hypericum perforatum, Symphytum officinale, Arnica montana |
| Administration Route(s): | ORAL |
| Dosage Form(s): | LIQUID |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57520-0512 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20100618 |
| Package NDC: | 57520-0512-1 |
| Package Description: | 30 mL in 1 BOTTLE, DROPPER (57520-0512-1) |
| NDC Code | 57520-0512-1 |
| Proprietary Name | Pre/Post Surgery |
| Package Description | 30 mL in 1 BOTTLE, DROPPER (57520-0512-1) |
| Product NDC | 57520-0512 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Hypericum perforatum, Symphytum officinale, Arnica montana |
| Dosage Form Name | LIQUID |
| Route Name | ORAL |
| Start Marketing Date | 20100618 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ARNICA MONTANA; COMFREY ROOT; HYPERICUM PERFORATUM |
| Strength Number | 200; 12; 12 |
| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| Pharmaceutical Classes |