Abropernol is a Oral Tablet in the Human Otc Drug category. It is labeled and distributed by Heel Inc. The primary component is Artemisia Abrotanum Flowering Top; Pulsatilla Vulgaris; Calcium Fluoride; Hamamelis Virginiana Root Bark/stem Bark; Amanita Muscaria Var. Muscaria Fruiting Body; Nitric Acid; Kerosene.
Product ID | 50114-6134_0183c6a7-6195-451c-9eef-81d60c769d4f |
NDC | 50114-6134 |
Product Type | Human Otc Drug |
Proprietary Name | Abropernol |
Generic 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 | Tablet |
Route of Administration | ORAL |
Marketing Start Date | 1984-01-31 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | ARTEMISIA ABROTANUM FLOWERING TOP; PULSATILLA VULGARIS; CALCIUM FLUORIDE; HAMAMELIS VIRGINIANA ROOT BARK/STEM BARK; AMANITA MUSCARIA VAR. MUSCARIA FRUITING BODY; NITRIC ACID; KEROSENE |
Active Ingredient Strength | 4 [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg; [hp_X]/300mg |
NDC Exclude Flag | E |
Listing Certified Through | 2017-12-31 |
Marketing Start Date | 1984-01-31 |
NDC Exclude Flag | N |
Sample Package? | N |
Marketing Category | unapproved homeopathic |
Product Type | HUMAN OTC DRUG |
Marketing Start Date | 1984-01-31 |
Inactivation Date | 2019-11-13 |
Ingredient | Strength |
---|---|
ARTEMISIA ABROTANUM FLOWERING TOP | 4 [hp_X]/300mg |
SPL SET ID: | adfe12ec-eea8-43a2-a283-45b1f63204a8 |
Manufacturer | |
UNII |
Mark Image Registration | Serial | Company Trademark Application Date |
---|---|
ABROPERNOL 73583979 1410101 Dead/Cancelled |
BIOLOGISCHE HEILMITTEL HEEL GMBH 1986-02-19 |