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    NDC 17089-0474-18 GUNA KIDNEY PLUS 12; 3; 6; 4; 3; 2; 6; 10; 2; 200; 6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL Details

    GUNA KIDNEY PLUS 12; 3; 6; 4; 3; 2; 6; 10; 2; 200; 6 [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL

    GUNA KIDNEY PLUS is a ORAL SOLUTION/ DROPS in the HUMAN OTC DRUG category. It is labeled and distributed by Guna spa. The primary component is APIS MELLIFERA; BERBERIS VULGARIS FRUIT; CALCIUM SULFIDE; CHONDRODENDRON TOMENTOSUM ROOT; EQUISETUM HYEMALE; HORSE CHESTNUT; LOBARIA PULMONARIA; SODIUM CHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA PITUITARY GLAND; URTICA URENS.

    Product Information

    NDC 17089-0474
    Product ID 17089-474_ba7eb1a4-9059-c47c-e053-2a95a90a6cce
    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 GUNA KIDNEY PLUS
    Proprietary Name Suffix n/a
    Non-Proprietary Name calcium sulfide - chondrodendron tomentosum root - equisetum hyemale - sus scrofa pituitary gland - apis mellifera - urtica urens - sodium chloride - lobaria pulmonaria - horse chestnut - berberis vulgaris fruit - solidago viragaurea flowering top -
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION/ DROPS
    Route ORAL
    Active Ingredient Strength 12; 3; 6; 4; 3; 2; 6; 10; 2; 200; 6
    Active Ingredient Units [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL
    Substance Name APIS MELLIFERA; BERBERIS VULGARIS FRUIT; CALCIUM SULFIDE; CHONDRODENDRON TOMENTOSUM ROOT; EQUISETUM HYEMALE; HORSE CHESTNUT; LOBARIA PULMONARIA; SODIUM CHLORIDE; SOLIDAGO VIRGAUREA FLOWERING TOP; SUS SCROFA PITUITARY GLAND; URTICA URENS
    Labeler Name Guna spa
    Pharmaceutical Class Allergens [CS], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Increased Large Intestinal Motility [PE], Inhibition Large Intestine Fluid/Electrolyte Absorption [PE], Osmotic Activity [MoA],
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 17089-0474-18 (17089047418)

    NDC Package Code 17089-474-18
    Billing NDC 17089047418
    Package 1 BOTTLE, DROPPER in 1 BOX (17089-474-18) / 30 mL in 1 BOTTLE, DROPPER
    Marketing Start Date 2021-01-17
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b8dacd94-8da1-4a8d-e053-2995a90acb67 Details

    Revised: 2/2021