| 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 |