Label: HEVERT DETOX LYMPH- arsenic trioxide, clematis recta flowering top, conium maculatum flowering top, lachesis muta venom, mercuric iodide, phytolacca americana root, toxicodendron pubescens shoot, scrophularia nodosa leaf with stem, and sulfur liquid

  • NDC Code(s): 54532-0034-5
  • Packager: Hevert Pharmaceuticals LLC
  • 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 July 11, 2018

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


    Drug Facts


    Active ingredientsPurpose
    "X" indicates a homeopathic dilution. For more information visit:
    Relief of discomfort associated with lymphatic swelling and edema
    Arsenicum album 6X*
    Clematis 4X*
    Conium 6X*
    Lachesis 8X*
    Mercurius bijodatus 8X*
    Phytolacca 4X*
    Rhus toxicodendron 6X*
    Scrophularia nodosa, herba 3X*
    Sulfur 4X*
  • Uses

    For temporary relief of discomfort associated with lymphatic swelling and edema.

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

  • Warnings

    For oral use only.

    Chronically enlarged lymph nodes can be the sign of different diseases. Therefore, consult a doctor in order to clarify the underlying disease before using this medicine. Also consult a doctor promptly in case of acute signs of inflammation (redness, heat, swelling, pain and dysfunction) and fever or enlargement of the lymph nodes during treatment.

    Do not use if

    • you are allergic to Rhus toxicodendron or other plants from the cashew family

    Stop use and ask a doctor if you suffer from thyroid disease or symptoms persist for more than 7 days, worsen or new symptoms occur.

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

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

  • Directions

    • Adults and children over 12 years of age: Take 20 drops in water 3 times daily.
    • Consult a physician for use in children under 12 years of age.
    • Do not use for children under 1 year of age.
  • Other information

    • Store at 68 to 77 °F.
    • Tamper Evident: Do not use if tamper evident strip is broken or missing from base of bottle cap.
    • To report serious adverse events, call 1-855-387-6466.
  • Inactive ingredients

    46 % ethanol V/V, purified water

  • Questions?



    Distributed by:
    Hevert Pharmaceuticals, LLC
    Boulder, CO 80303

  • PRINCIPAL DISPLAY PANEL - 50 ml Bottle Carton

    NDC 54532-0034-5

    Homeopathic Medicine

    For the lymphatic

    1.7 fl oz (50 ml)
    46 % alcohol V/V
    Oral drops

    Made in Germany


    Principal Display Panel - 50 ml Bottle Carton
    arsenic trioxide, clematis recta flowering top, conium maculatum flowering top, lachesis muta venom, mercuric iodide, phytolacca americana root, toxicodendron pubescens shoot, scrophularia nodosa leaf with stem, and sulfur liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:54532-0034
    Route of AdministrationORAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Arsenic Trioxide (UNII: S7V92P67HO) (Arsenic Cation (3+) - UNII:C96613F5AV) Arsenic Trioxide6 [hp_X]  in 50 mL
    Clematis Recta Flowering top (UNII: 396421SP9F) (Clematis Recta Flowering top - UNII:396421SP9F) Clematis Recta Flowering top4 [hp_X]  in 50 mL
    Conium Maculatum Flowering Top (UNII: Q28R5GF371) (Conium Maculatum Flowering Top - UNII:Q28R5GF371) Conium Maculatum Flowering Top6 [hp_X]  in 50 mL
    Lachesis Muta Venom (UNII: VSW71SS07I) (Lachesis Muta Venom - UNII:VSW71SS07I) Lachesis Muta Venom8 [hp_X]  in 50 mL
    Mercuric Iodide (UNII: R03O05RB0P) (Mercuric Iodide - UNII:R03O05RB0P) Mercuric Iodide8 [hp_X]  in 50 mL
    Phytolacca Americana Root (UNII: 11E6VI8VEG) (Phytolacca Americana Root - UNII:11E6VI8VEG) Phytolacca Americana Root4 [hp_X]  in 50 mL
    Toxicodendron Pubescens shoot (UNII: 46PYZ1F82M) (Toxicodendron Pubescens shoot - UNII:46PYZ1F82M) Toxicodendron Pubescens shoot6 [hp_X]  in 50 mL
    Scrophularia Nodosa leaf with stem (UNII: K93UPA2CNQ) (Scrophularia Nodosa leaf with stem - UNII:K93UPA2CNQ) Scrophularia Nodosa leaf with stem3 [hp_X]  in 50 mL
    Sulfur (UNII: 70FD1KFU70) (Sulfur - UNII:70FD1KFU70) Sulfur4 [hp_X]  in 50 mL
    Inactive Ingredients
    Ingredient NameStrength
    ALCOHOL (UNII: 3K9958V90M)  
    WATER (UNII: 059QF0KO0R)  
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:54532-0034-51 in 1 CARTON06/15/2016
    150 mL in 1 BOTTLE; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    Labeler - Hevert Pharmaceuticals LLC (078647622)
    Registrant - Hevert Arzneimittel GmbH & Co. KG (318100617)
    NameAddressID/FEIBusiness Operations
    Hevert Arzneimittel GmbH & Co. KG318100617MANUFACTURE(54532-0034)