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 |