| NDC Code | 48951-8379-1 |
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| Package Description | 10 AMPULE in 1 BOX (48951-8379-1) > 1 mL in 1 AMPULE |
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| Product NDC | 48951-8379 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Secale Betula |
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| Non-Proprietary Name | Secale Betula |
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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 | ARNICA MONTANA; BETULA PENDULA BARK; BETULA PENDULA LEAF; BOS TAURUS EYE; CLAVICEPS PURPUREA SCLEROTIUM; LEAD SULFIDE; LEVISTICUM OFFICINALE ROOT; TOBACCO LEAF |
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| Strength | 12; 4; 3; 8; 6; 8; 6; 6 |
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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], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Non-Standardized Plant Allergenic Extract [EPC], Plant Proteins [CS] |
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