| NDC Code | 63083-9235-1 |
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| Package Description | 29.5 mL in 1 BOTTLE, DROPPER (63083-9235-1) |
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| Product NDC | 63083-9235 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Nux Vomica Combination |
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| Proprietary Name Suffix | 9235 |
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| Non-Proprietary Name | Nux Vomica Combination |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 19840815 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | Professional Complementary Health Formulas |
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| Substance Name | BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; SULFUR |
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| Strength | 3; 6; 3; 3; 10 |
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| Strength Unit | [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL |
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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], Seed Storage Proteins [CS] |
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