| NDC Code | 48951-2042-1 |
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| Package Description | 10 AMPULE in 1 BOX (48951-2042-1) > 1 mL in 1 AMPULE |
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| Product NDC | 48951-2042 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Berberis Larix |
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| Non-Proprietary Name | Berberis Larix |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20090901 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | Uriel Pharmacy Inc. |
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| Substance Name | ACHILLEA MILLEFOLIUM; APIS MELLIFERA; BERBERIS VULGARIS ROOT BARK; EQUISETUM ARVENSE TOP; FERROUS DISULFIDE; LARIX DECIDUA RESIN; LYTTA VESICATORIA; SUS SCROFA URINARY BLADDER |
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| Strength | 3; 8; 3; 3; 8; 8; 6; 8 |
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| Strength Unit | [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL |
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| Pharmacy Classes | Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC] |
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