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    NDC 27281-0049-65 Immune Booster 200; 6; 6; 3; 200; 30; 3; 30; 200; 200 [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL Details

    Immune Booster 200; 6; 6; 3; 200; 30; 3; 30; 200; 200 [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL

    Immune Booster is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Sunway Biotech LLC. The primary component is APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; GALIUM APARINE; MERCURIC CHLORIDE; MERCURIC SULFIDE; MILK THISTLE; NITRIC ACID; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG.

    Product Information

    NDC 27281-0049
    Product ID 27281-049_d44c13ea-157e-a23c-e053-2995a90a4f07
    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 Immune Booster
    Proprietary Name Suffix n/a
    Non-Proprietary Name Apis mellifica, Baptisia tinctoria, Carduus marianus, Echinacea angustifolia, Gallum aparine, Mercurius corrosivus, Mercurius sulphuratus ruber, Nitricum acidum, Sulphur iodatum, Thuja occidentalis.
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 200; 6; 6; 3; 200; 30; 3; 30; 200; 200
    Active Ingredient Units [hp_C]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_X]/30mL; [hp_C]/30mL; [hp_C]/30mL; [hp_C]/30mL
    Substance Name APIS MELLIFERA; BAPTISIA TINCTORIA ROOT; ECHINACEA ANGUSTIFOLIA; GALIUM APARINE; MERCURIC CHLORIDE; MERCURIC SULFIDE; MILK THISTLE; NITRIC ACID; SULFUR IODIDE; THUJA OCCIDENTALIS LEAFY TWIG
    Labeler Name Sunway Biotech LLC
    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 2024-12-31

    Package

    NDC 27281-0049-65 (27281004965)

    NDC Package Code 27281-049-65
    Billing NDC 27281004965
    Package 30 mL in 1 BOTTLE, SPRAY (27281-049-65)
    Marketing Start Date 2013-11-13
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9ae14a66-9f6b-4ca8-b335-f6f75ddb8d93 Details

    Revised: 12/2021