| Product NDC: | 50114-4262 |
| Proprietary Name: | Back |
| Non Proprietary Name: | CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM and AMMONIUM CHLORIDE and GELSEMIUM SEMPERVIRENS ROOT and TOXICODENDRON PUBESCENS LEAF and ARSENIC TRIOXIDE and MATRICARIA RECUTITA and |
| Active Ingredient(s): | 6; 10; 5; 6; 10; 5; 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 & nbsp; CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM and AMMONIUM CHLORIDE and GELSEMIUM SEMPERVIRENS ROOT and TOXICODENDRON PUBESCENS LEAF and ARSENIC TRIOXIDE and MATRICARIA RECUTITA and |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50114-4262 |
| Labeler Name: | Heel Inc. |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20070830 |
| Package NDC: | 50114-4262-2 |
| Package Description: | 100 TABLET in 1 BOTTLE (50114-4262-2) |
| NDC Code | 50114-4262-2 |
| Proprietary Name | Back |
| Package Description | 100 TABLET in 1 BOTTLE (50114-4262-2) |
| Product NDC | 50114-4262 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | CITRULLUS COLOCYNTHIS FRUIT PULP and PSEUDOGNAPHALIUM OBTUSIFOLIUM and AMMONIUM CHLORIDE and GELSEMIUM SEMPERVIRENS ROOT and TOXICODENDRON PUBESCENS LEAF and ARSENIC TRIOXIDE and MATRICARIA RECUTITA and |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20070830 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc. |
| Substance Name | AMMONIUM CHLORIDE; ARSENIC TRIOXIDE; CITRULLUS COLOCYNTHIS FRUIT PULP; GELSEMIUM SEMPERVIRENS ROOT; MATRICARIA RECUTITA; PSEUDOGNAPHALIUM OBTUSIFOLIUM; TOXICODENDRON PUBESCENS LEAF |
| Strength Number | 6; 10; 5; 6; 10; 5; 8 |
| Strength Unit | [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
| Pharmaceutical Classes |