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 |