| 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 |