| NDC Code | 44911-0725-1 |
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| Package Description | 30 mL in 1 BOTTLE, DROPPER (44911-0725-1) |
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| Product NDC | 44911-0725 |
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| Product Type Name | HUMAN OTC DRUG |
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| Proprietary Name | Household Antigens |
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| Non-Proprietary Name | Acetone, Sodium Tripolyphosphate, Propylene Glycol, Benzinum, Ammonium Muriaticum, Sodium Lauryl Sulfate, Terebinthina, Butyl Acetate, Ethyl Acetate, Toluene, Xylene, Bisphenol A, Petroleum, Formalinum, Glyphosate, Methylparaben, Naphthalinum, Propylparaben, Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla (pratensis), Sulphur, Paraffinum |
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| Dosage Form | LIQUID |
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| Usage | ORAL |
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| Start Marketing Date | 20241220 |
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| Marketing Category Name | UNAPPROVED HOMEOPATHIC |
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| Manufacturer | Energique, Inc. |
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| Substance Name | ACETONE; AMMONIUM CHLORIDE; BENZENE; BISPHENOL A; BUTYL ACETATE; ETHYL ACETATE; FORMALDEHYDE SOLUTION; GLYPHOSATE; GRAPHITE; KEROSENE; METHYLPARABEN; NAPHTHALENE; NITRIC ACID; PARAFFIN; PROPYLENE GLYCOL; PROPYLPARABEN; PULSATILLA PRATENSIS WHOLE; SEMECARPUS ANACARDIUM JUICE; SODIUM LAURYL SULFATE; SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM; SULFUR; TOLUENE; TURPENTINE OIL; XYLENE (MIXED ISOMERS) |
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| Strength | 9; 9; 9; 9; 9; 9; 9; 9; 12; 9; 9; 9; 12; 12; 9; 9; 12; 12; 9; 9; 12; 9; 9; 9 |
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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_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], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC], Standardized Chemical Allergen [EPC] |
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