Label: RHUSTOXOFORCE- apis mellifica, cantharis, graphites, natrum muriaticum, rhus glabra, rhus toxicodendron, 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 December 2, 2015

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  • ACTIVE INGREDIENTS:

    Apis Mellifica 12X, Cantharis 12X, Graphites 12X, Natrum Muriaticum 12X, Rhus Glabra 12X, Rhus Toxidodendron 12X, Rhus Venenata 12X, Urtica Dioica 12X

  • INDICATIONS:

    For temporary relief of allergies caused by poison ivy, oak, and summac.

  • WARNINGS:

    ​If pregnant or breast-feeding,​ ask a health care professional befure 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.

  • DIRECTIONS:

    10 drops orally, 3 times a day. Consult a physician for use in children under 12 years of age.

  • INACTIVE INGREDIENTS:

    Demineralized Water, 25% 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:

    For temporary relief of allergies caused by poison ivy, oak, and summac.

  • QUESTIONS:

    Distributed by:

    BIOACTIVE NUTRITIONAL

    Melbourne, FL 32935

    For Nutritional Information write:

    BioActive Nutritional, Inc.

    1803 N. Wickham Rd.

    Melbourne, Fl 32935

  • PACKAGE LABEL DISPLAY:

    BioActie Homeopathic

    RHUSTOXOFORCE

    1 FL OZ (30 mL)

    Rhustoxoforce

  • INGREDIENTS AND APPEARANCE
    RHUSTOXOFORCE 
    apis mellifica, cantharis, graphites, natrum muriaticum, rhus glabra, rhus toxicodendron, rhus venenata, urtica dioica liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43857-0206
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    APIS MELLIFERA (UNII: 7S82P3R43Z) (APIS MELLIFERA - UNII:7S82P3R43Z) APIS MELLIFERA12 [hp_X]  in 1 mL
    LYTTA VESICATORIA (UNII: 3Q034RO3BT) (LYTTA VESICATORIA - UNII:3Q034RO3BT) LYTTA VESICATORIA12 [hp_X]  in 1 mL
    GRAPHITE (UNII: 4QQN74LH4O) (GRAPHITE - UNII:4QQN74LH4O) GRAPHITE12 [hp_X]  in 1 mL
    SODIUM CHLORIDE (UNII: 451W47IQ8X) (CHLORIDE ION - UNII:Q32ZN48698) SODIUM CHLORIDE12 [hp_X]  in 1 mL
    RHUS GLABRA TOP (UNII: RHH784E0K6) (RHUS GLABRA TOP - UNII:RHH784E0K6) RHUS GLABRA TOP12 [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:43857-0206-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/21/2013
    Labeler - BioActive Nutritional, Inc. (624980496)
    Registrant - Apotheca Company (844330915)
    Establishment
    NameAddressID/FEIBusiness Operations
    Apotheca Company844330915manufacture(43857-0206) , api manufacture(43857-0206) , label(43857-0206) , pack(43857-0206)
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