Label: CONTACT ALLERGY ANTIGEN- toxicodendron diversilobum leaf, toxicodendron pubescens leaf, toxicodendron vernix leafy twig, urtica dioica, semecarpus anacardium juice, graphite, daphne mezereum bark, urtica urens, xerophyllum asphodeloides 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 May 26, 2020

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

  • ACTIVE INGREDIENT

    ACTIVE INGREDIENTS - equal amounts of: Rhus Divers 9X, 12X, 15X, 30X, Rhus Tox 9X, 12X, 15X, 30X, Rhus Ven 9X, 12X, 15X, 30X, Urtica Di 9x, 12X, 15X, 30X, Anacard Or 12X, Graphites 12X, Mezereum 12X, Urtica Ur 12X, Xerophyllum 12X.

  • PURPOSE

    USES: Temporarily relieves occasional skin irritation.**

  • INDICATIONS & USAGE

    USES: Temporarily relieves occasional skin irritation.**

  • DOSAGE & ADMINISTRATION

    DIRECTIONS: Adults & children above 12 years: 10 drops orally 3 times daily, or as directed by a health care professional.

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.

  • WARNINGS

    WARNINGS:

    • Consult a physician for use in children under 12 years of age.
    • IF PREGNANT OR BREAST-FEEDING, ask a health care professional before use.
    • KEEP OUT OF THE REACH OF CHILDREN. In case of overdose (or accidental ingestion) get medical help or contact a Poison Control Center right away.
    • Do not use if TAMPER EVIDENT seal is broken or missing.
  • INACTIVE INGREDIENT

    INACTIVE INGREDIENTS: Ethyl Alcohol USP, Purified Water.

  • QUESTIONS

    QUESTIONS & COMMENTS?

    Natural Creations, Inc. / Woodbine, IA 51579 / 712-647-1600

  • REFERENCES

    * The letters "HPUS" indicate the components in the product are officially monographed in the Homeopathic Pharmacopeia of the United States.

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

  • PRINCIPAL DISPLAY PANEL

    NDC: 43406-0115-1

    CONTACT ALLERGY ANTIGEN

    HOMEOPATHIC

    1 fl oz (3o mL) / 20% alcohol

    UPC: 87773001047   NON GMO Logo

    image description

  • INGREDIENTS AND APPEARANCE
    CONTACT ALLERGY ANTIGEN 
    toxicodendron diversilobum leaf, toxicodendron pubescens leaf, toxicodendron vernix leafy twig, urtica dioica, semecarpus anacardium juice, graphite, daphne mezereum bark, urtica urens, xerophyllum asphodeloides liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:43406-0115
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (TOXICODENDRON DIVERSILOBUM LEAF - UNII:V727AWD6ZZ) TOXICODENDRON DIVERSILOBUM LEAF30 [hp_X]  in 1 mL
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF30 [hp_X]  in 1 mL
    TOXICODENDRON VERNIX LEAFY TWIG (UNII: Y3VW699H96) (TOXICODENDRON VERNIX LEAFY TWIG - UNII:Y3VW699H96) TOXICODENDRON VERNIX LEAFY TWIG30 [hp_X]  in 1 mL
    URTICA DIOICA (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46) URTICA DIOICA30 [hp_X]  in 1 mL
    SEMECARPUS ANACARDIUM FRUIT (UNII: 7399B063X9) (SEMECARPUS ANACARDIUM FRUIT - UNII:7399B063X9) SEMECARPUS ANACARDIUM FRUIT12 [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
    URTICA URENS (UNII: IHN2NQ5OF9) (URTICA URENS - UNII:IHN2NQ5OF9) URTICA URENS12 [hp_X]  in 1 mL
    XEROPHYLLUM ASPHODELOIDES (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES12 [hp_X]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:43406-0115-130 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product01/01/2010
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic01/01/2010
    Labeler - Natural Creations, Inc. (018022074)
    Establishment
    NameAddressID/FEIBusiness Operations
    OHM Pharma, Inc.030572478manufacture(43406-0115)