| Product ID | 63083-9235_61685066-ac8a-418a-a914-d91494749211 |
| NDC | 63083-9235 |
| Product Type | Human Otc Drug |
| Proprietary Name | Nux Vomica Combination 9235 |
| Generic Name | Nux Vomica Combination |
| Dosage Form | Liquid |
| Route of Administration | ORAL |
| Marketing Start Date | 1984-08-15 |
| Marketing Category | UNAPPROVED HOMEOPATHIC / |
| Labeler Name | Professional Complementary Health Formulas |
| Substance Name | BRYONIA ALBA ROOT; CITRULLUS COLOCYNTHIS FRUIT PULP; LYCOPODIUM CLAVATUM SPORE; STRYCHNOS NUX-VOMICA SEED; SULFUR |
| Active Ingredient Strength | 3 [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL; [hp_X]/29.5mL |
| Pharm 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] |
| NDC Exclude Flag | N |
| Listing Certified Through | 2023-12-31 |