Nectadyn - 50114-8510-1 - (DROSERA ROTUNDIFOLIA and IPECAC and RUMEX CRISPUS ROOT and ANTIMONY POTASSIUM TARTRATE and CUPRIC SULFATE and SPONGIA OFFICINALIS SKELETON, ROASTED)

Alphabetical Index


Drug Information of Nectadyn

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)

Labeler Information of Nectadyn

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 Information of Nectadyn

Package NDC: 50114-8510-1
Package Description: 1 BOTTLE in 1 CARTON (50114-8510-1) > 125 mL in 1 BOTTLE

NDC Information of Nectadyn

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

Complete Information of Nectadyn


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