Product NDC: | 50114-6110 |
Proprietary Name: | Oculoheel |
Non Proprietary Name: | SPIGELIA ANTHELMIA and CALCIUM SULFIDE and TOXICODENDRON PUBESCENS LEAF and DELPHINIUM STAPHISAGRIA SEED and APIS MELLIFERA and SODIUM CHLORIDE and MERCURIC SULFIDE |
Active Ingredient(s): | 4; 12; 4; 8; 6; 6; 12 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp; SPIGELIA ANTHELMIA and CALCIUM SULFIDE and TOXICODENDRON PUBESCENS LEAF and DELPHINIUM STAPHISAGRIA SEED and APIS MELLIFERA and SODIUM CHLORIDE and MERCURIC SULFIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-6110 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19840131 |
Package NDC: | 50114-6110-2 |
Package Description: | 30000 mg in 1 BOTTLE (50114-6110-2) |
NDC Code | 50114-6110-2 |
Proprietary Name | Oculoheel |
Package Description | 30000 mg in 1 BOTTLE (50114-6110-2) |
Product NDC | 50114-6110 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | SPIGELIA ANTHELMIA and CALCIUM SULFIDE and TOXICODENDRON PUBESCENS LEAF and DELPHINIUM STAPHISAGRIA SEED and APIS MELLIFERA and SODIUM CHLORIDE and MERCURIC SULFIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19840131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | APIS MELLIFERA; CALCIUM SULFIDE; DELPHINIUM STAPHISAGRIA SEED; MERCURIC SULFIDE; SODIUM CHLORIDE; SPIGELIA ANTHELMIA; TOXICODENDRON PUBESCENS LEAF |
Strength Number | 4; 12; 4; 8; 6; 6; 12 |
Strength Unit | [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg |
Pharmaceutical Classes |