Product NDC: | 50114-1200 |
Proprietary Name: | Berberis Homaccord |
Non Proprietary Name: | CITRULLUS COLOCYNTHIS FRUIT PULP and BERBERIS VULGARIS ROOT BARK and VERATRUM ALBUM ROOT |
Active Ingredient(s): | 2; 3; 3 [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL & nbsp; CITRULLUS COLOCYNTHIS FRUIT PULP and BERBERIS VULGARIS ROOT BARK and VERATRUM ALBUM ROOT |
Administration Route(s): | ORAL |
Dosage Form(s): | LIQUID |
Coding System: | National Drug Codes(NDC) |
Product NDC: | 50114-1200 |
Labeler Name: | Heel Inc |
Product Type: | HUMAN OTC DRUG |
FDA Application Number: | |
Marketing Category: | UNAPPROVED HOMEOPATHIC |
Start Marketing Date: | 19860131 |
Package NDC: | 50114-1200-4 |
Package Description: | 50 mL in 1 BOTTLE (50114-1200-4) |
NDC Code | 50114-1200-4 |
Proprietary Name | Berberis Homaccord |
Package Description | 50 mL in 1 BOTTLE (50114-1200-4) |
Product NDC | 50114-1200 |
Product Type Name | HUMAN OTC DRUG |
Non Proprietary Name | CITRULLUS COLOCYNTHIS FRUIT PULP and BERBERIS VULGARIS ROOT BARK and VERATRUM ALBUM ROOT |
Dosage Form Name | LIQUID |
Route Name | ORAL |
Start Marketing Date | 19860131 |
Marketing Category Name | UNAPPROVED HOMEOPATHIC |
Labeler Name | Heel Inc |
Substance Name | BERBERIS VULGARIS ROOT BARK; CITRULLUS COLOCYNTHIS FRUIT PULP; VERATRUM ALBUM ROOT |
Strength Number | 2; 3; 3 |
Strength Unit | [hp_X]/50mL; [hp_X]/50mL; [hp_X]/50mL |
Pharmaceutical Classes |