Label: HOUSEHOLD ANTIGENS- acetone, sodium tripolyphosphate, propylene glycol, sodium benzene sulfonate, sodium lauryl sulfate, terebinthina, liquid

  • 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 August 7, 2012

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  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS: Household Antigens 9X, 12X, 15X, 30X, Anacardium Orientale 12X, 15X, Grephites 12X, 15X, Nitriucm Acidum 12X, 15X, Pulsatilla 12X, 15X, Sulphur 15X.

  • PURPOSE

    INDICATIONS: For temporary relief of allergies due to household chemicals.

  • WARNINGS

    WARNINGS: If pregnant or breast-feeding, ask a health professional before use.

    Keep out of reach of children. In case of overdose, get medical help or contact a Poison Control Center right away.

    Do not use if tamper evident seal is broken or missing.

    Store in a cool, dry place.

  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care porfessional. If symptoms persist, consult your health care professional. Consult a physician for use in children under 12 years of age.

  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN. In case of overdose, get medical help or contact a Poison Control Center right away.

  • INDICATIONS & USAGE

    INDICATIONS: For temporary relief of allergies due to household chemicals.

  • QUESTIONS

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579

    800-869-8078

  • PRINCIPAL DISPLAY PANEL

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    HOUSEHOLD ANTIGENS

    1 fl. oz (30 ml)

    Household Antigens

  • INGREDIENTS AND APPEARANCE
    HOUSEHOLD ANTIGENS 
    acetone, sodium tripolyphosphate, propylene glycol, sodium benzene sulfonate, sodium lauryl sulfate, terebinthina, liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0017
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ACETONE (UNII: 1364PS73AF) (ACETONE - UNII:1364PS73AF) ACETONE9 [hp_X]  in 1 mL
    SODIUM TRIPOLYPHOSPHATE (UNII: 5HK03SA80J) (TRIPOLYPHOSPHATE ION - UNII:5798IYA5AY) SODIUM TRIPOLYPHOSPHATE9 [hp_X]  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL9 [hp_X]  in 1 mL
    SODIUM BENZENESULFONATE (UNII: K5RM14AZHX) (SODIUM BENZENESULFONATE - UNII:K5RM14AZHX) SODIUM BENZENESULFONATE9 [hp_X]  in 1 mL
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CHLORIDE9 [hp_X]  in 1 mL
    SODIUM LAURYL SULFATE (UNII: 368GB5141J) (LAURYL SULFATE - UNII:DIQ16UC154) SODIUM LAURYL SULFATE9 [hp_X]  in 1 mL
    TURPENTINE OIL (UNII: C5H0QJ6V7F) (TURPENTINE OIL - UNII:C5H0QJ6V7F) TURPENTINE OIL9 [hp_X]  in 1 mL
    BUTYL ACETATE (UNII: 464P5N1905) (BUTYL ACETATE - UNII:464P5N1905) BUTYL ACETATE9 [hp_X]  in 1 mL
    TOLUENE (UNII: 3FPU23BG52) (TOLUENE - UNII:3FPU23BG52) TOLUENE9 [hp_X]  in 1 mL
    XYLENE (UNII: D856J1047R) (XYLENE - UNII:D856J1047R) XYLENE9 [hp_X]  in 1 mL
    DIBUTYL PHTHALATE (UNII: 2286E5R2KE) (DIBUTYL PHTHALATE - UNII:2286E5R2KE) DIBUTYL PHTHALATE9 [hp_X]  in 1 mL
    KEROSENE (UNII: 1C89KKC04E) (KEROSENE - UNII:1C89KKC04E) KEROSENE9 [hp_X]  in 1 mL
    SEMECARPUS ANACARDIUM JUICE (UNII: Y0F0BU8RDU) (SEMECARPUS ANACARDIUM JUICE - UNII:Y0F0BU8RDU) SEMECARPUS ANACARDIUM JUICE12 [hp_X]  in 1 mL
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE12 [hp_X]  in 1 mL
    NITRIC ACID (UNII: 411VRN1TV4) (NITRIC ACID - UNII:411VRN1TV4) NITRIC ACID12 [hp_X]  in 1 mL
    PULSATILLA VULGARIS (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS12 [hp_X]  in 1 mL
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR12 [hp_X]  in 1 mL
    ETHYL ACETATE (UNII: 76845O8NMZ) (ETHYL ACETATE - UNII:76845O8NMZ) ETHYL ACETATE9 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    Water (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0017-130 mL in 1 BOTTLE, DROPPER
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/07/2012
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0017)
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