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    NDC 50181-0065-01 Lymph Detox Plus 3; 3; 3; 6; 3; 5; 12; 4; 3; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL Details

    Lymph Detox Plus 3; 3; 3; 6; 3; 5; 12; 4; 3; 6 [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL

    Lymph Detox Plus is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by The Wellness Center for Research and Education, Inc.. The primary component is APIS MELLIFERA; ARNICA MONTANA; BERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; SOLIDAGO VIRGAUREA FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF.

    Product Information

    NDC 50181-0065
    Product ID 50181-0065_dc587745-4106-4cbe-a156-fa20798de54e
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Lymph Detox Plus
    Proprietary Name Suffix n/a
    Non-Proprietary Name Apis Mellifica, Arnica Montana, Berberis Vulgaris, Gelsemium Sempervirens, Solidago Virgaurea, Phytolacca Decandra, Hydrastis Canadensis, Chelidonium Majus, Rhus Tox, Lachesis Mutus
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 3; 3; 3; 6; 3; 5; 12; 4; 3; 6
    Active Ingredient Units [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL; [hp_X]/mL
    Substance Name APIS MELLIFERA; ARNICA MONTANA; BERBERIS VULGARIS ROOT BARK; CHELIDONIUM MAJUS; GELSEMIUM SEMPERVIRENS ROOT; GOLDENSEAL; LACHESIS MUTA VENOM; PHYTOLACCA AMERICANA ROOT; SOLIDAGO VIRGAUREA FLOWERING TOP; TOXICODENDRON PUBESCENS LEAF
    Labeler Name The Wellness Center for Research and Education, Inc.
    Pharmaceutical Class Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Standardized Insect Venom Allergenic Extract [EPC]
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2023-12-31

    Package

    NDC 50181-0065-01 (50181006501)

    NDC Package Code 50181-0065-1
    Billing NDC 50181006501
    Package 30 mL in 1 BOTTLE, DROPPER (50181-0065-1)
    Marketing Start Date 2019-05-02
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL fe5d0979-037d-4f43-ae06-8469c85ee504 Details

    Revised: 3/2022