Label: POISON IVY/OAK 1013- poison ivy/oak 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 15, 2019

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

  • ACTIVE INGREDIENTS

    Echinacea purpurea 2X
    Adrenal 6X
    ACTH 6X, 30X
    Liver 6X, 12X
    Croton tiglium 8X
    Histaminum hydrochloricum 12X
    Kreosotum 12X
    Xerophyllum 12X
    and all the following at 6X, 12X, 60X, 100X:
    Rhus diversiloba (poison oak)
    Rhus toxicodendron (poison ivy)
    Stinging nettle
    Sumac

  • QUESTIONS

    Professional Formulas

    PO Box 2034 Lake Oswego, OR 97035

  • INDICATIONS

    For the temporary relief of redness, swelling, stinging, itching of skin, and itching of nose or throat due to sensitivity to poison ivy and poison oak.*

  • PURPOSE

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

  • WARNINGS

    Severe symptoms such as difficulty breathing, facial swelling, dizziness, confusion, and hives may be life-threatening and require immediate emergency care. Keep out of the reach of children. In case of overdose, get medical help or contact a poison control center right away. If pregnant or breastfeeding, ask a healthcare professional before use.

    Keep out of the reach of children.

    If pregnant or breastfeeding, ask a healthcare professional before use.

  • DIRECTIONS

    Place drops under tongue 30 minutes before/after meals. Adults and children 12 years and over: Take 10 to 15 drops up to 3 times per day. For desensitization, begin with 1 to 5 drops daily, increasing to the standard dose gradually to avoid symptom expression; after 1 to 3 months at the standard dose, decrease gradually to a maintenance dose of 10 to 15 drops weekly. Consult a physician for use in children under 12 years of age.

  • OTHER INFORMATION

    Tamper resistant. If seal is broken, do not use. After opening, close container tightly and store at room temperature away from heat.

  • INACTIVE INGREDIENTS

    20% ethanol, purified water.

  • LABEL

    Est 1985

    Professional Formulas

    Complementary Health

    Poison Ivy/Oak

    Homeopathic Remedy

    2 FL. OZ. (59 mL)

    Label image

  • INGREDIENTS AND APPEARANCE
    POISON IVY/OAK  1013
    poison ivy/oak liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63083-1013
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ECHINACEA PURPUREA WHOLE (UNII: QI7G114Y98) (ECHINACEA PURPUREA WHOLE - UNII:QI7G114Y98) ECHINACEA PURPUREA WHOLE2 [hp_X]  in 59 mL
    SUS SCROFA ADRENAL GLAND (UNII: 398IYQ16YV) (SUS SCROFA ADRENAL GLAND - UNII:398IYQ16YV) SUS SCROFA ADRENAL GLAND6 [hp_X]  in 59 mL
    CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA) CORTICOTROPIN6 [hp_X]  in 59 mL
    BEEF LIVER (UNII: W8N8R55022) (BEEF LIVER - UNII:W8N8R55022) BEEF LIVER6 [hp_X]  in 59 mL
    CROTON TIGLIUM SEED (UNII: 0HK2GZK66E) (CROTON TIGLIUM SEED - UNII:0HK2GZK66E) CROTON TIGLIUM SEED8 [hp_X]  in 59 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 59 mL
    WOOD CREOSOTE (UNII: 3JYG22FD73) (WOOD CREOSOTE - UNII:3JYG22FD73) WOOD CREOSOTE12 [hp_X]  in 59 mL
    XEROPHYLLUM ASPHODELOIDES WHOLE (UNII: 9I4XB1GP2B) (XEROPHYLLUM ASPHODELOIDES WHOLE - UNII:9I4XB1GP2B) XEROPHYLLUM ASPHODELOIDES WHOLE12 [hp_X]  in 59 mL
    TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (TOXICODENDRON DIVERSILOBUM LEAF - UNII:V727AWD6ZZ) TOXICODENDRON DIVERSILOBUM LEAF6 [hp_X]  in 59 mL
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF6 [hp_X]  in 59 mL
    URTICA DIOICA SUBSP. DIOICA LEAF (UNII: 232L6DS3Y4) (URTICA DIOICA SUBSP. DIOICA LEAF - UNII:232L6DS3Y4) URTICA DIOICA SUBSP. DIOICA LEAF6 [hp_X]  in 59 mL
    AILANTHUS ALTISSIMA FRUIT (UNII: 0W913N2K5N) (AILANTHUS ALTISSIMA FRUIT - UNII:0W913N2K5N) AILANTHUS ALTISSIMA FRUIT6 [hp_X]  in 59 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:63083-1013-259 mL in 1 BOTTLE, DROPPER; Type 0: Not a Combination Product08/15/1985
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic08/15/1984
    Labeler - Professional Complementary Health Formulas (167339027)
    Registrant - Natural Pharmaceutical Manufacturing (015624923)
    Establishment
    NameAddressID/FEIBusiness Operations
    Natural Pharmaceutical Manufacturing015624923manufacture(63083-1013)