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

If you are a consumer or patient please visit this version.

  • 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.

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  • PURPOSE

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

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  • 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.

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  • 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.

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  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: Demineralized water, 20% Ethanol.

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  • 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.

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  • INDICATIONS & USAGE

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

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  • QUESTIONS

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579

    800-869-8078

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  • PRINCIPAL DISPLAY PANEL

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    HOUSEHOLD ANTIGENS

    1 fl. oz (30 ml)

    Household Antigens

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  • INGREDIENTS AND APPEARANCE
    HOUSEHOLD ANTIGENS 
    acetone, sodium tripolyphosphate, propylene glycol, sodium benzene sulfonate, sodium lauryl sulfate, terebinthina, liquid
    Product 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) (SODIUM BENZENESULFONATE - UNII:K5RM14AZHX) SODIUM BENZENESULFONATE 9 [hp_X]  in 1 mL
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CHLORIDE 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 (UNII: D856J1047R) (XYLENE - UNII:D856J1047R) XYLENE 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 (UNII: I76KB35JEV) (PULSATILLA VULGARIS - UNII:I76KB35JEV) PULSATILLA VULGARIS 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
    Marketing Information
    Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date
    unapproved homeopathic 08/07/2012
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    Name Address ID/FEI Business Operations
    Apotheca Company 844330915 manufacture(44911-0017)
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