Label: HENDEL RHUS TOX- toxicodendron pubescens leaf tablet

  • 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 22, 2022

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  • WARNINGS

    If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If symptoms persist or worsen, a health professional should be consulted. Do not use if sensitivity to Rhus Tox 6X, 12X, 30X, 200X or any of its ingredients exists. In case of accidental overdose, contact a Poison Control Center immediately.

  • USES

    For the temporary relief of:
    • Painful Joints
    • Muscle Aches
    • Stiffness in Joints

  • KEEP OUT OF REACH OF CHILDREN

    KEEP OUT OF REACH OF CHILDREN

  • DIRECTIONS

    Adults 18 and over: 1 tablet sublingually or dissolved completely in mouth 2 to 3 times per day or as directed by a physician

  • INDICATIONS

    Painful Joints, Muscle Aches, Stiffness in Joints

  • INACTIVE INGREDIENT

    Lactose, Magnesium stearate

  • INGREDIENTS

    Each tablet contains equal parts of Rhus Tox 6X, 12X, 30X, 200X.

  • PRINCIPAL DISPLAY PANEL

    Hendel Rhus Tox

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  • INGREDIENTS AND APPEARANCE
    HENDEL RHUS TOX 
    toxicodendron pubescens leaf tablet
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:62795-1127
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF6 [hp_X]
    Inactive Ingredients
    Ingredient NameStrength
    MAGNESIUM STEARATE (UNII: 70097M6I30)  
    LACTOSE MONOHYDRATE (UNII: EWQ57Q8I5X)  
    Product Characteristics
    ColorwhiteScoreno score
    ShapeROUNDSize9mm
    FlavorImprint Code LEAFMAN
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62795-1127-2100 in 1 BOTTLE; Type 0: Not a Combination Product07/12/201601/31/2027
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic07/12/201601/31/2027
    Labeler - MediNatura Inc (079324099)
    Establishment
    NameAddressID/FEIBusiness Operations
    MediNatura Inc102783016manufacture(62795-1127)
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