| Product NDC: | 50114-4336 |
| Proprietary Name: | Asthma Rx |
| Non Proprietary Name: | ARSENIC TRIOXIDE and ACTIVATED CHARCOAL and SULFUR |
| Active Ingredient(s): | 12; 12; 12 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp; ARSENIC TRIOXIDE and ACTIVATED CHARCOAL and SULFUR |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50114-4336 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN PRESCRIPTION DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 20111130 |
| Package NDC: | 50114-4336-2 |
| Package Description: | 30000 mg in 1 BOTTLE (50114-4336-2) |
| NDC Code | 50114-4336-2 |
| Proprietary Name | Asthma Rx |
| Package Description | 30000 mg in 1 BOTTLE (50114-4336-2) |
| Product NDC | 50114-4336 |
| Product Type Name | HUMAN PRESCRIPTION DRUG |
| Non Proprietary Name | ARSENIC TRIOXIDE and ACTIVATED CHARCOAL and SULFUR |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 20111130 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | ACTIVATED CHARCOAL; ARSENIC TRIOXIDE; SULFUR |
| Strength Number | 12; 12; 12 |
| Strength Unit | [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg |
| Pharmaceutical Classes |