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    NDC 27281-0029-63 Livergen 3; 200; 8; 200; 6; 1; 6; 8; 2 [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL Details

    Livergen 3; 200; 8; 200; 6; 1; 6; 8; 2 [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL

    Livergen is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Sunway Biotech LLC. The primary component is ARNICA MONTANA; BRYONIA ALBA ROOT; CERVUS ELAPHUS HORN OIL; CHELIDONIUM MAJUS; HERRING SPERM DNA; MILK THISTLE; PORK LIVER; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE.

    Product Information

    NDC 27281-0029
    Product ID 27281-029_d44c110b-8910-67a2-e053-2a95a90a6a03
    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 Livergen
    Proprietary Name Suffix n/a
    Non-Proprietary Name Arnica montana, Bryonia, Carduus marianus, Chelidonium majus, DNA, Hepar suis, Oleum animale, Pancreas suis, Taraxacum officinale.
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 3; 200; 8; 200; 6; 1; 6; 8; 2
    Active Ingredient Units [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
    Substance Name ARNICA MONTANA; BRYONIA ALBA ROOT; CERVUS ELAPHUS HORN OIL; CHELIDONIUM MAJUS; HERRING SPERM DNA; MILK THISTLE; PORK LIVER; SUS SCROFA PANCREAS; TARAXACUM OFFICINALE
    Labeler Name Sunway Biotech LLC
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 27281-0029-63 (27281002963)

    NDC Package Code 27281-029-63
    Billing NDC 27281002963
    Package 30 mL in 1 PACKAGE (27281-029-63)
    Marketing Start Date 2013-11-13
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 0e72f898-9685-47c9-b617-00145254bf8c Details

    Revised: 12/2021