Product NDC: | 50114-6005 |
Proprietary Name: | Aletris - Heel |
Non Proprietary Name: | SEPIA OFFICINALIS JUICE and ALETRIS FARINOSA ROOT and ANAMIRTA COCCULUS SEED and CHAMAELIRIUM LUTEUM ROOT and POTASSIUM CARBONATE and SODIUM CHLORIDE and QUININE ARSENATE and PICRIC ACID and |
Active Ingredient(s): | 4; 4; 4; 6; 4; 6; 6; 6 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; SEPIA OFFICINALIS JUICE and ALETRIS FARINOSA ROOT and ANAMIRTA COCCULUS SEED and CHAMAELIRIUM LUTEUM ROOT and POTASSIUM CARBONATE and SODIUM CHLORIDE and QUININE ARSENATE and PICRIC ACID and |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-6005 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19840131 |
Package NDC: | 50114-6005-2 |
Package Description: | 100 TABLET in 1 BOTTLE (50114-6005-2) |
NDC Code | 50114-6005-2 |
Proprietary Name | Aletris - Heel |
Package Description | 100 TABLET in 1 BOTTLE (50114-6005-2) |
Product NDC | 50114-6005 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SEPIA OFFICINALIS JUICE and ALETRIS FARINOSA ROOT and ANAMIRTA COCCULUS SEED and CHAMAELIRIUM LUTEUM ROOT and POTASSIUM CARBONATE and SODIUM CHLORIDE and QUININE ARSENATE and PICRIC ACID and |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19840131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | ALETRIS FARINOSA ROOT; ANAMIRTA COCCULUS SEED; CHAMAELIRIUM LUTEUM ROOT; PICRIC ACID; POTASSIUM CARBONATE; QUININE ARSENATE; SEPIA OFFICINALIS JUICE; SODIUM CHLORIDE |
Strength Number | 4; 4; 4; 6; 4; 6; 6; 6 |
Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
Pharmaceutical Classes |