Label: RHUS TOXICODENDRON MT- rhus toxicodendron tincture

  • 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 29, 2021

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

  • ACTIVE INGREDIENT

    Active Ingredient: Rhus Toxicodendron MT

  • INDICATIONS & USAGE

  • WARNINGS

    Caution: for manufacturing,

    processing or repacking only.

  • DOSAGE & ADMINISTRATION

  • OTHER SAFETY INFORMATION

    Batch no. 40945

    Retest Date: 08/2023

  • INACTIVE INGREDIENT

    Inactive Ingredient: Ethanol 49%, Purified Water

  • QUESTIONS

    Distributed by: OHM Pharma

    Mineral Wells, TX 76067

    www.ohmpharma.com

  • PRINCIPAL DISPLAY PANEL

    ​NDC 66096-752-08

    Rhus Toxicodendron MT

    0.250 Liters

    ​Caution: for manufacturing,

    processing or repacking only.

    Active Ingredient: Rhus Toxicodendron MT

    Inactive Ingredient: Ethanol 49%, Purified Water

    Batch no. 40945

    Retest Date: 08/2023

    Distributed by: OHM Pharma

    Mineral Wells, TX 76067

    www.ohmpharma.com

    Rhus Toxicodendron MT

  • INGREDIENTS AND APPEARANCE
    RHUS TOXICODENDRON MT 
    rhus toxicodendron tincture
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:66096-752
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    TOXICODENDRON PUBESCENS LEAF (UNII: 6IO182RP7A) (TOXICODENDRON PUBESCENS LEAF - UNII:6IO182RP7A) TOXICODENDRON PUBESCENS LEAF1 [hp_X]  in 0.25 L
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:66096-752-080.25 L in 1 BOTTLE; Type 0: Not a Combination Product03/01/2019
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved homeopathic03/01/2019
    Labeler - OHM PHARMA INC. (030572478)
    Registrant - OHM PHARMA INC. (030572478)
    Establishment
    NameAddressID/FEIBusiness Operations
    OHM PHARMA INC.030572478manufacture(66096-752)