| Product NDC: | 50114-8510 |
| Proprietary Name: | Nectadyn |
| Non Proprietary Name: | DROSERA ROTUNDIFOLIA and IPECAC and RUMEX CRISPUS ROOT and ANTIMONY POTASSIUM TARTRATE and CUPRIC SULFATE and SPONGIA OFFICINALIS SKELETON, ROASTED |
| Active Ingredient(s): | 6; 6; 4; 4; 4; 8 [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL & nbsp; DROSERA ROTUNDIFOLIA and IPECAC and RUMEX CRISPUS ROOT and ANTIMONY POTASSIUM TARTRATE and CUPRIC SULFATE and SPONGIA OFFICINALIS SKELETON, ROASTED |
| Administration Route(s): | ORAL |
| Dosage Form(s): | SYRUP |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50114-8510 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20070831 |
| Package NDC: | 50114-8510-1 |
| Package Description: | 1 BOTTLE in 1 CARTON (50114-8510-1) > 125 mL in 1 BOTTLE |
| NDC Code | 50114-8510-1 |
| Proprietary Name | Nectadyn |
| Package Description | 1 BOTTLE in 1 CARTON (50114-8510-1) > 125 mL in 1 BOTTLE |
| Product NDC | 50114-8510 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | DROSERA ROTUNDIFOLIA and IPECAC and RUMEX CRISPUS ROOT and ANTIMONY POTASSIUM TARTRATE and CUPRIC SULFATE and SPONGIA OFFICINALIS SKELETON, ROASTED |
| Dosage Form Name | SYRUP |
| Route Name | ORAL |
| Start Marketing Date | 20070831 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | ANTIMONY POTASSIUM TARTRATE; CUPRIC SULFATE; DROSERA ROTUNDIFOLIA; IPECAC; RUMEX CRISPUS ROOT; SPONGIA OFFICINALIS SKELETON, ROASTED |
| Strength Number | 6; 6; 4; 4; 4; 8 |
| Strength Unit | [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL; [hp_X]/125mL |
| Pharmaceutical Classes |