Product NDC: | 50114-6010 |
Proprietary Name: | Apis compositum |
Non Proprietary Name: | TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE |
Active Ingredient(s): | 4; 8; 6; 6; 4; 6; 4 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp; TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE |
Administration Route(s): | ORAL |
Dosage Form(s): | TABLET |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-6010 |
Labeler Name: | Heel Inc. |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19840131 |
Package NDC: | 50114-6010-2 |
Package Description: | 30000 mg in 1 BOTTLE (50114-6010-2) |
NDC Code | 50114-6010-2 |
Proprietary Name | Apis compositum |
Package Description | 30000 mg in 1 BOTTLE (50114-6010-2) |
Product NDC | 50114-6010 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | TURPENTINE OIL and NUTMEG and APIS MELLIFERA and STRYCHNOS IGNATII SEED and VERATRUM ALBUM ROOT and PHOSPHORUS and MERCURIC CHLORIDE |
Dosage Form Name | TABLET |
Route Name | ORAL |
Start Marketing Date | 19840131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc. |
Substance Name | APIS MELLIFERA; MERCURIC CHLORIDE; NUTMEG; PHOSPHORUS; STRYCHNOS IGNATII SEED; TURPENTINE OIL; VERATRUM ALBUM ROOT |
Strength Number | 4; 8; 6; 6; 4; 6; 4 |
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 |