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    NDC 17089-0467-20 GUNA DEFENSE 10; 4; 2; 2; 4; 10; 6; 6 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g Details

    GUNA DEFENSE 10; 4; 2; 2; 4; 10; 6; 6 [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g

    GUNA DEFENSE is a ORAL PELLET in the HUMAN OTC DRUG category. It is labeled and distributed by Guna spa. The primary component is CALCIUM SULFIDE; CENTELLA ASIATICA; ECHINACEA ANGUSTIFOLIA WHOLE; ECHINACEA PURPUREA; PHYTOLACCA AMERICANA ROOT; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; VINCETOXICUM HIRUNDINARIA ROOT.

    Product Information

    NDC 17089-0467
    Product ID 17089-467_d32e09c7-895a-2b2d-e053-2a95a90a6eee
    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 DEFENSE
    Proprietary Name Suffix n/a
    Non-Proprietary Name calcium sulfide - centella asiatica - echinacea angustifolia whole - echinacea purpurea - thuja occidentalis leafy twig - vincetoxicum hirundinaria root - phytolacca americana root - sulfur -
    Product Type HUMAN OTC DRUG
    Dosage Form PELLET
    Route ORAL
    Active Ingredient Strength 10; 4; 2; 2; 4; 10; 6; 6
    Active Ingredient Units [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g; [hp_X]/4g
    Substance Name CALCIUM SULFIDE; CENTELLA ASIATICA; ECHINACEA ANGUSTIFOLIA WHOLE; ECHINACEA PURPUREA; PHYTOLACCA AMERICANA ROOT; SULFUR; THUJA OCCIDENTALIS LEAFY TWIG; VINCETOXICUM HIRUNDINARIA ROOT
    Labeler Name Guna spa
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 17089-0467-20 (17089046720)

    NDC Package Code 17089-467-20
    Billing NDC 17089046720
    Package 2 TUBE in 1 BOX (17089-467-20) / 4 g in 1 TUBE
    Marketing Start Date 2020-09-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL af94b281-be4f-4715-e053-2995a90af153 Details

    Revised: 12/2021