Label: POLLUTOX- 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, ozone, uranium nitricum liquid
- NDC Code(s): 43742-2095-1
- Packager: Deseret Biologicals, Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
- Marketing Status: unapproved homeopathic
DISCLAIMER: This homeopathic product has not been evaluated by the Food and Drug Administration for safety or efficacy. FDA is not aware of scientific evidence to support homeopathy as effective.
Drug Label Information
Updated March 27, 2024
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ACTIVE INGREDIENTS:
Acetone 12X, 15X, 30X, Arsenicum Album 12X, Benzinum 12X, Berberis Vulgaris 8X, Cadmium Sulphuratum 12X, Carbon Dioxide 12X, 15X, 30X, Chlorinum 12X, 15X, 30X, Hydrofluoricum Acidum 12X, Melatonin 12X, Mercurius Solubilis 12X, 15X, 30X, Nitrogenum Oxygenatum 12X, Nux Vomica 12X, Ozone 16X, Petroleum 12X, Plumbum Metallicum 12X, Stannum Metallicum 12X, Sulphuricum Acidum 6X, 12X, 30X, Toluene 12X, Uranium Nitricum 15C.
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PURPOSE:
Acetone-Head Pain, Arsenicum Album - Nausea, Benzinum – Head Pain, Berberis Vulgaris – Head Pain, Cadmium Sulphuratum – Abdominal Pain, Carbon Dioxide - Nausea, Chlorinum – Head Pain, Hydrofluoricum Acidum – Abdominal Pain, Melatonin - Fatigue, Mercurius Solubilis - Nausea, Nitrogenum Oxygenatum - Fatigue, Nux Vomica - Fatigue, Ozone – Head Pain, Petroleum - Fatigue, Plumbum Metallicum – Abdominal Pain, Stannum Metallicum – Abdominal Pain, Sulphuricum Acidum - Nausea, Toluene - Fatigue, Uranium Nitricum – Head Pain
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INGREDIENTS AND APPEARANCE
POLLUTOX
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, ozone, uranium nitricum liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:43742-2095 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength SULFURIC ACID (UNII: O40UQP6WCF) (SULFURIC ACID - UNII:O40UQP6WCF) SULFURIC ACID 6 [hp_X] in 1 mL BERBERIS VULGARIS ROOT BARK (UNII: 1TH8Q20J0U) (BERBERIS VULGARIS ROOT BARK - UNII:1TH8Q20J0U) BERBERIS VULGARIS ROOT BARK 8 [hp_X] in 1 mL ARSENIC TRIOXIDE (UNII: S7V92P67HO) (ARSENIC CATION (3+) - UNII:C96613F5AV) ARSENIC TRIOXIDE 12 [hp_X] in 1 mL BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F) BENZENE 12 [hp_X] in 1 mL CADMIUM SULFIDE (UNII: 057EZR4Z7Q) (CADMIUM CATION - UNII:T494FZ4G8G) CADMIUM SULFIDE 12 [hp_X] in 1 mL HYDROFLUORIC ACID (UNII: RGL5YE86CZ) (FLUORIDE ION - UNII:Q80VPU408O) FLUORIDE ION 12 [hp_X] in 1 mL MELATONIN (UNII: JL5DK93RCL) (MELATONIN - UNII:JL5DK93RCL) MELATONIN 12 [hp_X] in 1 mL NITROUS OXIDE (UNII: K50XQU1029) (NITROUS OXIDE - UNII:K50XQU1029) NITROUS OXIDE 12 [hp_X] in 1 mL STRYCHNOS NUX-VOMICA SEED (UNII: 269XH13919) (STRYCHNOS NUX-VOMICA SEED - UNII:269XH13919) STRYCHNOS NUX-VOMICA SEED 12 [hp_X] in 1 mL KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 12 [hp_X] in 1 mL LEAD (UNII: 2P299V784P) (LEAD - UNII:2P299V784P) LEAD 12 [hp_X] in 1 mL TIN (UNII: 387GMG9FH5) (TIN - UNII:387GMG9FH5) TIN 12 [hp_X] in 1 mL TOLUENE (UNII: 3FPU23BG52) (TOLUENE - UNII:3FPU23BG52) TOLUENE 12 [hp_X] in 1 mL ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF) ACETONE 12 [hp_X] in 1 mL CARBON DIOXIDE (UNII: 142M471B3J) (CARBON DIOXIDE - UNII:142M471B3J) CARBON DIOXIDE 12 [hp_X] in 1 mL CHLORINE (UNII: 4R7X1O2820) (CHLORINE - UNII:4R7X1O2820) CHLORINE 12 [hp_X] in 1 mL MERCURIUS SOLUBILIS (UNII: 324Y4038G2) (MERCURIUS SOLUBILIS - UNII:324Y4038G2) MERCURIUS SOLUBILIS 12 [hp_X] in 1 mL OZONE (UNII: 66H7ZZK23N) (OZONE - UNII:66H7ZZK23N) OZONE 16 [hp_X] in 1 mL URANYL NITRATE HEXAHYDRATE (UNII: 3V057702FY) (URANIUM CATION (6+) - UNII:5PI36AS4G7) URANYL NITRATE HEXAHYDRATE 15 [hp_C] in 1 mL Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALCOHOL (UNII: 3K9958V90M) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:43742-2095-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 10/13/2023 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 10/13/2023 Labeler - Deseret Biologicals, Inc. (940741853) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(43742-2095) , api manufacture(43742-2095) , label(43742-2095) , pack(43742-2095)
