Label: POISON IVY AND OAK FORMULA (glandula suprarenalis- bovine, hepar suis, rhus tox, urtica dioica, rhus aromatica, rhus glabra, histaminum hydrochloricum, rhus diversiloba, adrenocorticotrophin spray

  • NDC Code(s): 83027-0039-1
  • Packager: Nutritional Specialties, Inc.
  • 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 29, 2023

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  • ACTIVE INGREDIENTS:

    Glandula Suprarenalis (Bovine) 6X, 12X, Hepar Suis (Liver) 6X, 12X, Rhus Tox (Poison Ivy) 6X, 12X, 60X, 100X, Urtica Dioica (Stinging Nettle) 6X, 12X, 60X, 100X, Rhus Aromatica (Fragrant Sumac) 8X, 12X, 60X, 100X, Rhus Glabra 8X, 12X, 60X, 100X, Histaminum Hydrochloricum 12X, Rhus Diversiloba (Pacific Poison Oak) 16X, 30X, 60X, 100X, Adrenocorticotrophin 15C, 30C.

  • PURPOSE:

    Provides factors that mitigate hypersensitivity to poison ivy and poison oak.

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

  • WARNINGS:

    Professional Use Only

    If pregnant or breast-feeding, ask a health professional before use.

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

    If condition worsens, seek medical attention.

    KEEP OUT OF REACH OF CHILDREN

    Do not use if tamper evident seal is broken or missing.

    Store in a cool place after opening

  • 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: 2 to 3 sprays orally, three times daily. Children under twelve one half adult dosage. Do not take within 15 minutes of consuming food, beverage or brushing teeth. Consult a physician for use in children under 12 years of age.

  • INDICATIONS:

    Provides factors that mitigate hypersensitivity to poison ivy and poison oak.†
    †Claims based on traditional homeopathic practice, not accepted medical evidence. Not FDA evaluated.

  • INACTIVE INGREDIENTS:

    Alcohol USP 20%, Purified Water USP.

  • QUESTIONS:

    MANUFACTURED EXCLUSIVELY FOR

    NUTRITIONAL SPECIALTIES, INC.

    PO BOX 97227

    PITTSBURG, PA 15229

    www.phpltd.com

  • PACKAGE LABEL DISPLAY:

    Professional

    Health Products

    HOMEOPATHIC

    NDC 83027-0039-1

    POISON IVY &

    OAK FORMULA

    2 FL. OZ (60 ml)

    POISON IVY & OAK FORMULA

  • INGREDIENTS AND APPEARANCE
    POISON IVY AND OAK FORMULA 
    glandula suprarenalis (bovine), hepar suis, rhus tox, urtica dioica, rhus aromatica, rhus glabra, histaminum hydrochloricum, rhus diversiloba, adrenocorticotrophin spray
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83027-0039
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BOS TAURUS ADRENAL GLAND (UNII: M2776SWB29) (BOS TAURUS ADRENAL GLAND - UNII:M2776SWB29) BOS TAURUS ADRENAL GLAND6 [hp_X]  in 1 mL
    PORK LIVER (UNII: 6EC706HI7F) (PORK LIVER - UNII:6EC706HI7F) PORK LIVER6 [hp_X]  in 1 mL
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF6 [hp_X]  in 1 mL
    URTICA DIOICA WHOLE (UNII: 710FLW4U46) (URTICA DIOICA - UNII:710FLW4U46) URTICA DIOICA WHOLE6 [hp_X]  in 1 mL
    RHUS AROMATICA ROOT BARK (UNII: Q3H36W0J42) (RHUS AROMATICA ROOT BARK - UNII:Q3H36W0J42) RHUS AROMATICA ROOT BARK8 [hp_X]  in 1 mL
    RHUS GLABRA TOP (UNII: RHH784E0K6) (RHUS GLABRA TOP - UNII:RHH784E0K6) RHUS GLABRA TOP8 [hp_X]  in 1 mL
    HISTAMINE DIHYDROCHLORIDE (UNII: 3POA0Q644U) (HISTAMINE - UNII:820484N8I3) HISTAMINE DIHYDROCHLORIDE12 [hp_X]  in 1 mL
    TOXICODENDRON DIVERSILOBUM LEAF (UNII: V727AWD6ZZ) (TOXICODENDRON DIVERSILOBUM LEAF - UNII:V727AWD6ZZ) TOXICODENDRON DIVERSILOBUM LEAF16 [hp_X]  in 1 mL
    CORTICOTROPIN (UNII: K0U68Q2TXA) (CORTICOTROPIN - UNII:K0U68Q2TXA) CORTICOTROPIN15 [hp_C]  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ALCOHOL (UNII: 3K9958V90M)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83027-0039-160 mL in 1 BOTTLE, SPRAY; Type 0: Not a Combination Product03/29/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/29/2023
    Labeler - Nutritional Specialties, Inc. (032744609)
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