| NDC Code | 43742-2037-1 |
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| Package Description | 30 mL in 1 BOTTLE, DROPPER (43742-2037-1) |
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| Product NDC | 43742-2037 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Pollutox |
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| Non-Proprietary Name | Sulphuricum Acidum, Berberis Vulgaris, Arsenicum Album, Benzinum, Cadmium Sulphuratum, Hydrofluoricum Acidum, Melatonin, Nitrogenum Oxygenatum, Nux Vomica, Petroleum, Plumbum Metallicum, Stannum Metallicum, Toluene, Acetone, Carbon Dioxide, Chlorinum, Mercurius Solubilis, Uranium Nitricum, Ozone |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20230721 |
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| End Marketing Date | 20270718 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | Deseret Biologicals, Inc. |
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| Substance Name | SULFURIC ACID; BERBERIS VULGARIS ROOT BARK; ARSENIC TRIOXIDE; BENZENE; CADMIUM SULFIDE; HYDROFLUORIC ACID; MELATONIN; NITROUS OXIDE; STRYCHNOS NUX-VOMICA SEED; KEROSENE; LEAD; TIN; TOLUENE; ACETONE; CARBON DIOXIDE; CHLORINE; MERCURIUS SOLUBILIS; URANYL NITRATE HEXAHYDRATE; OZONE |
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| Strength | 12; 12; 12; 8; 12; 12; 12; 12; 12; 12; 12; 12; 12; 16; 12; 6; 12; 12; 15 |
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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; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_C]/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], Radiographic Contrast Agent [EPC], Seed Storage Proteins [CS], X-Ray Contrast Activity [MoA] |
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