| Product NDC: | 50114-6134 |
| Proprietary Name: | Abropernol |
| Non Proprietary Name: | ARTEMISIA ABROTANUM FLOWERING TOP and PULSATILLA VULGARIS and CALCIUM FLUORIDE and HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK and AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY and NITRIC ACID and KEROSEN |
| Active Ingredient(s): | 5; 4; 12; 4; 6; 6; 4 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg & nbsp; ARTEMISIA ABROTANUM FLOWERING TOP and PULSATILLA VULGARIS and CALCIUM FLUORIDE and HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK and AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY and NITRIC ACID and KEROSEN |
| Administration Route(s): | ORAL |
| Dosage Form(s): | TABLET |
| Coding System: | National Drug Codes(NDC) |
| Product NDC: | 50114-6134 |
| Labeler Name: | Heel Inc |
| Product Type: | HUMAN OTC DRUG |
| FDA Application Number: | |
| Marketing Category: | UNAPPROVED HOMEOPATHIC |
| Start Marketing Date: | 19840131 |
| Package NDC: | 50114-6134-2 |
| Package Description: | 30000 mg in 1 BOTTLE (50114-6134-2) |
| NDC Code | 50114-6134-2 |
| Proprietary Name | Abropernol |
| Package Description | 30000 mg in 1 BOTTLE (50114-6134-2) |
| Product NDC | 50114-6134 |
| Product Type Name | HUMAN OTC DRUG |
| Non Proprietary Name | ARTEMISIA ABROTANUM FLOWERING TOP and PULSATILLA VULGARIS and CALCIUM FLUORIDE and HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK and AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY and NITRIC ACID and KEROSEN |
| Dosage Form Name | TABLET |
| Route Name | ORAL |
| Start Marketing Date | 19840131 |
| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
| Labeler Name | Heel Inc |
| Substance Name | AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY; ARTEMISIA ABROTANUM FLOWERING TOP; CALCIUM FLUORIDE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; KEROSENE; NITRIC ACID; PULSATILLA VULGARIS |
| Strength Number | 5; 4; 12; 4; 6; 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 |