| 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; SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM; PROPYLENE GLYCOL; BENZENE; AMMONIUM CHLORIDE; SODIUM LAURYL SULFATE; TURPENTINE OIL; BUTYL ACETATE; ETHYL ACETATE; TOLUENE; XYLENE (MIXED ISOMERS); BISPHENOL A; KEROSENE; FORMALDEHYDE SOLUTION; GLYPHOSATE; METHYLPARABEN; NAPHTHALENE; PROPYLPARABEN; SEMECARPUS ANACARDIUM JUICE; GRAPHITE; NITRIC ACID; PULSATILLA PRATENSIS WHOLE; SULFUR; PARAFFIN |
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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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