Label: CONTACT ALLERGY ANTIGENS- anacardium orientale, graphites, mezereum, xerophyllum asphodeloides, rhus diversiloba, rhus tox, rhus venenata, urtica dioica 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 March 23, 2022

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

  • ACTIVE INGREDIENTS:

    Anacardium Orientale 12X, 15X, Graphites 12X, 15X, Mezereum 12X, 15X, Xerophyllum Asphodeloides 12X, 15X, Rhus Diversiloba 12X, 15X, 18X, 30X, Rhus Tox 12X, 15X, 18X, 30X, Rhus Venenata 12X, 15X, 18X, 30X, Urtica Dioica 12X, 15X, 18X, 30X.

  • INDICATIONS:

    May temporarily relieve symptoms associated with poison ivy, poison oak, poison sumac, and stinging nettle allergies.**

    **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:

    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, consult your health care professional. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    May temporarily relieve symptoms associated with poison ivy, poison oak, poison sumac, and stinging nettle allergies.**

    **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
    CONTACT ALLERGY
    ANTIGENS
    1 fl. oz. (30 ml)

    Contact Allergy Antigens

  • INGREDIENTS AND APPEARANCE
    CONTACT ALLERGY ANTIGENS 
    anacardium orientale, graphites, mezereum, xerophyllum asphodeloides, rhus diversiloba, rhus tox, rhus venenata, urtica dioica liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:44911-0297
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    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
    DAPHNE MEZEREUM BARK (UNII: X2N6E405GV) (DAPHNE MEZEREUM BARK - UNII:X2N6E405GV) DAPHNE MEZEREUM BARK12 [hp_X]  in 1 mL
    XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES12 [hp_X]  in 1 mL
    TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (TOXICODENDRON DIVERSILOBUM LEAF - UNII:V727AWD6ZZ) TOXICODENDRON DIVERSILOBUM LEAF12 [hp_X]  in 1 mL
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF12 [hp_X]  in 1 mL
    TOXICODENDRON VERNIX LEAFY TWIG (UNII: Y3VW699H96) (TOXICODENDRON VERNIX LEAFY TWIG - UNII:Y3VW699H96) TOXICODENDRON VERNIX LEAFY TWIG12 [hp_X]  in 1 mL
    URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46) URTICA DIOICA12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:44911-0297-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product11/18/201504/04/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic11/18/201504/04/2023
    Labeler - Energique, Inc. (789886132)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(44911-0297) , api manufacture(44911-0297) , label(44911-0297) , pack(44911-0297)