Label: HOUSEHOLD ANTIGENS (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 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 December 20, 2024

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

  • ACTIVE INGREDIENTS:

    (in each drop): 6.66% of Anacardium Orientale, Graphites, Nitricum Acidum, Pulsatilla, Sulphur 12X, 15X; Paraffinum 12X, 15X, 30X. 1.67% of Household Allersodes (Acetone, Ammonium Muriaticum, Benzinum, Bisphenol A, Butyl Acetate, Ethyl Acetate, Petroleum, Propylene Glycol, Sodium Lauryl Sulfate, Sodium Tripolyphosphate, Terebinthina, Toluene, Xylene), Household Allersodes II (Formalinum, Glyphosate, Methylparaben, Naphthalinum, Propylparaben), 9X, 12X, 15X, 30X.

  • PURPOSE:

    May temporarily relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • 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.

  • KEEP OUT OF REACH OF CHILDREN:

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

  • DIRECTIONS:

    Adults and children 5 to 10 drops orally, 3 times daily or as otherwise directed by a health care professional. If symptoms persist for more than 7 days, consult your health care professional. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    May temporarily relieve symptoms associated with household chemicals sensitivities, such as dizziness and headache.**

    **Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • INACTIVE INGREDIENTS:

    Demineralized water, 20% Ethanol.

  • QUESTIONS:

    Dist. by Energique, Inc.

    201 Apple Blvd

    Woodbine, IA 51579

    800-869-8078

  • PACKAGE LABEL DISPLAY:

    ENERGIQUE

    since 1987

    HOMEOPATHIC REMEDY

    HOUSEHOLD ANTIGENS

    1 fl. oz (30 ml)

    HOUSEHOLD ANTIGENS

  • INGREDIENTS AND APPEARANCE
    HOUSEHOLD ANTIGENS 
    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 liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0725
    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, UNSPECIFIED FORM (UNII: 5HK03SA80J) (TRIPOLYPHOSPHATE ION - UNII:5798IYA5AY) SODIUM TRIPOLYPHOSPHATE, UNSPECIFIED FORM9 [hp_X]  in 1 mL
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) (PROPYLENE GLYCOL - UNII:6DC9Q167V3) PROPYLENE GLYCOL9 [hp_X]  in 1 mL
    BENZENE (UNII: J64922108F) (BENZENE - UNII:J64922108F) BENZENE9 [hp_X]  in 1 mL
    AMMONIUM CHLORIDE (UNII: 01Q9PC255D) (AMMONIUM CATION - UNII:54S68520I4) AMMONIUM CATION9 [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
    ETHYL ACETATE (UNII: 76845O8NMZ) (ETHYL ACETATE - UNII:76845O8NMZ) ETHYL ACETATE9 [hp_X]  in 1 mL
    TOLUENE (UNII: 3FPU23BG52) (TOLUENE - UNII:3FPU23BG52) TOLUENE9 [hp_X]  in 1 mL
    XYLENE (MIXED ISOMERS) (UNII: D856J1047R) (XYLENE - UNII:D856J1047R) XYLENE (MIXED ISOMERS)9 [hp_X]  in 1 mL
    BISPHENOL A (UNII: MLT3645I99) (BISPHENOL A - UNII:MLT3645I99) BISPHENOL A9 [hp_X]  in 1 mL
    KEROSENE (UNII: 1C89KKC04E) (DEODORIZED KEROSENE - UNII:1C89KKC04E) KEROSENE9 [hp_X]  in 1 mL
    FORMALDEHYDE SOLUTION (UNII: T0H3L6C7I5) (FORMALDEHYDE SOLUTION - UNII:T0H3L6C7I5) FORMALDEHYDE SOLUTION9 [hp_X]  in 1 mL
    GLYPHOSATE (UNII: 4632WW1X5A) (GLYPHOSATE - UNII:4632WW1X5A) GLYPHOSATE9 [hp_X]  in 1 mL
    METHYLPARABEN (UNII: A2I8C7HI9T) (METHYLPARABEN - UNII:A2I8C7HI9T) METHYLPARABEN9 [hp_X]  in 1 mL
    NAPHTHALENE (UNII: 2166IN72UN) (NAPHTHALENE - UNII:2166IN72UN) NAPHTHALENE9 [hp_X]  in 1 mL
    PROPYLPARABEN (UNII: Z8IX2SC1OH) (PROPYLPARABEN - UNII:Z8IX2SC1OH) PROPYLPARABEN9 [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 PRATENSIS WHOLE (UNII: 8E272251DI) (PULSATILLA PRATENSIS WHOLE - UNII:8E272251DI) PULSATILLA PRATENSIS WHOLE12 [hp_X]  in 1 mL
    SULFUR (UNII: 70FD1KFU70) (SULFUR - UNII:70FD1KFU70) SULFUR12 [hp_X]  in 1 mL
    PARAFFIN (UNII: I9O0E3H2ZE) (PARAFFIN - UNII:I9O0E3H2ZE) PARAFFIN12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0725-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product12/20/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic12/20/2024
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0725) , api manufacture(44911-0725) , label(44911-0725) , pack(44911-0725)