Label: HOUSEHOLD ANTIGENS- acetone, sodium tripolyphosphate, propylene glycol, sodium benzene sulfonate, sodium lauryl sulfate, terebinthina, liquid
- NDC Code(s): 44911-0017-1
- Packager: Energique, 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 July 20, 2020
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- ACTIVE INGREDIENT
- PURPOSE
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- INACTIVE INGREDIENT
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INGREDIENTS AND APPEARANCE
HOUSEHOLD ANTIGENS
acetone, sodium tripolyphosphate, propylene glycol, sodium benzene sulfonate, sodium lauryl sulfate, terebinthina, liquidProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:44911-0017 Route of Administration ORAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF) ACETONE 9 [hp_X] in 1 mL SODIUM TRIPOLYPHOSPHATE (UNII: 5HK03SA80J) (TRIPOLYPHOSPHATE ION - UNII:5798IYA5AY) SODIUM TRIPOLYPHOSPHATE 9 [hp_X] in 1 mL PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL 9 [hp_X] in 1 mL SODIUM BENZENESULFONATE (UNII: K5RM14AZHX) (BENZENESULFONIC ACID - - UNII:685928Z18A) SODIUM BENZENESULFONATE 9 [hp_X] in 1 mL AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION 9 [hp_X] in 1 mL SODIUM LAURYL SULFATE (UNII: 368GB5141J) (LAURYL SULFATE - UNII:DIQ16UC154) SODIUM LAURYL SULFATE 9 [hp_X] in 1 mL TURPENTINE OIL (UNII: C5H0QJ6V7F) (TURPENTINE OIL - UNII:C5H0QJ6V7F) TURPENTINE OIL 9 [hp_X] in 1 mL BUTYL ACETATE (UNII: 464P5N1905) (BUTYL ACETATE - UNII:464P5N1905) BUTYL ACETATE 9 [hp_X] in 1 mL TOLUENE (UNII: 3FPU23BG52) (TOLUENE - UNII:3FPU23BG52) TOLUENE 9 [hp_X] in 1 mL XYLENE (MIXED ISOMERS) (UNII: D856J1047R) (XYLENE - UNII:D856J1047R) XYLENE (MIXED ISOMERS) 9 [hp_X] in 1 mL DIBUTYL PHTHALATE (UNII: 2286E5R2KE) (DIBUTYL PHTHALATE - UNII:2286E5R2KE) DIBUTYL PHTHALATE 9 [hp_X] in 1 mL KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE 9 [hp_X] in 1 mL SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (SEMECARPUS ANACARDIUM JUICE - UNII:Y0F0BU8RDU) SEMECARPUS ANACARDIUM JUICE 12 [hp_X] in 1 mL GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE 12 [hp_X] in 1 mL NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID 12 [hp_X] in 1 mL PULSATILLA VULGARIS WHOLE (UNII: I76KB35JEV) (ANEMONE PULSATILLA - UNII:I76KB35JEV) PULSATILLA VULGARIS WHOLE 12 [hp_X] in 1 mL SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR 12 [hp_X] in 1 mL ETHYL ACETATE (UNII: 76845O8NMZ) (ETHYL ACETATE - UNII:76845O8NMZ) ETHYL ACETATE 9 [hp_X] 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:44911-0017-1 30 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product 08/07/2012 08/10/2021 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved homeopathic 08/07/2012 08/10/2021 Labeler - Energique, Inc. (789886132) Registrant - Apotheca Company (844330915) Establishment Name Address ID/FEI Business Operations Apotheca Company 844330915 manufacture(44911-0017) , api manufacture(44911-0017) , label(44911-0017) , pack(44911-0017)