NDC 48951-2119
Berberis Larix
Berberis Larix
Berberis Larix is a Oral Pellet in the Human Otc Drug category. It is labeled and distributed by Uriel Pharmacy Inc. The primary component is Achillea Millefolium; Berberis Vulgaris Root Bark; Equisetum Arvense Top; Lytta Vesicatoria; Apis Mellifera; Larix Decidua Resin.
Product ID | 48951-2119_6d94f4d0-0a7a-b284-e053-2a91aa0ab707 |
NDC | 48951-2119 |
Product Type | Human Otc Drug |
Proprietary Name | Berberis Larix |
Generic Name | Berberis Larix |
Dosage Form | Pellet |
Route of Administration | ORAL |
Marketing Start Date | 2009-09-01 |
Marketing Category | UNAPPROVED HOMEOPATHIC / UNAPPROVED HOMEOPATHIC |
Labeler Name | Uriel Pharmacy Inc |
Substance Name | ACHILLEA MILLEFOLIUM; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; LYTTA VESICATORIA; APIS MELLIFERA; LARIX DECIDUA RESIN |
Active Ingredient Strength | 3 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 |
NDC Exclude Flag | N |
Listing Certified Through | 2020-12-31 |