| 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 |