NDC 48951-2042
Berberis Larix
Berberis Larix
Berberis Larix is a Oral Liquid 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; Ferrous Disulfide; Larix Decidua Resin; Sus Scrofa Urinary Bladder.
| Product ID | 48951-2042_6cb8e31b-5222-aac5-e053-2a91aa0aa2fc |
| NDC | 48951-2042 |
| Product Type | Human Otc Drug |
| Proprietary Name | Berberis Larix |
| Generic Name | Berberis Larix |
| Dosage Form | Liquid |
| 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; FERROUS DISULFIDE; LARIX DECIDUA RESIN; SUS SCROFA URINARY BLADDER |
| Active Ingredient Strength | 3 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
| NDC Exclude Flag | N |
| Listing Certified Through | 2020-12-31 |