| 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 |