| Product NDC: | 57520-0398 |
| Proprietary Name: | Zyvestra |
| Non Proprietary Name: | Cocculus indicus, Ferrum metallicum, Gelsemium sempervirens, Phytolacca decandra, Pulsatilla, Silicea, |
| Active Ingredient(s): | 55; 55; 55; 55; 55 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; Cocculus indicus, Ferrum metallicum, Gelsemium sempervirens, Phytolacca decandra, Pulsatilla, Silicea, |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 57520-0398 |
| Labeler Name: | Apotheca Company |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20101203 |
| Package NDC: | 57520-0398-1 |
| Package Description: | 60 TABLET in 1 BOTTLE (57520-0398-1) |
| NDC Code | 57520-0398-1 |
| Proprietary Name | Zyvestra |
| Package Description | 60 TABLET in 1 BOTTLE (57520-0398-1) |
| Product NDC | 57520-0398 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | Cocculus indicus, Ferrum metallicum, Gelsemium sempervirens, Phytolacca decandra, Pulsatilla, Silicea, |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20101203 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Apotheca Company |
| Substance Name | ANAMIRTA COCCULUS SEED; GELSEMIUM SEMPERVIRENS ROOT; IRON; PHYTOLACCA AMERICANA ROOT; SILICON DIOXIDE |
| Strength Number | 55; 55; 55; 55; 55 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |