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 |