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    NDC 68703-0315-30 Migo-Ease 30; 6; 6; 6; 6 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1 Details

    Migo-Ease 30; 6; 6; 6; 6 [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1

    Migo-Ease is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Silver Star Brands. The primary component is ACONITUM NAPELLUS; LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED.

    Product Information

    NDC 68703-0315
    Product ID 68703-315_f61eec61-48ba-a3cb-e053-2995a90a7db2
    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 Migo-Ease
    Proprietary Name Suffix n/a
    Non-Proprietary Name Aconitum nap, Lycopodium, Nat mur, Nux vom, Pulsatilla
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 30; 6; 6; 6; 6
    Active Ingredient Units [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1; [hp_C]/1
    Substance Name ACONITUM NAPELLUS; LYCOPODIUM CLAVATUM SPORE; PULSATILLA VULGARIS; SODIUM CHLORIDE; STRYCHNOS NUX-VOMICA SEED
    Labeler Name Silver Star Brands
    Pharmaceutical Class Allergens [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], Non-Standardized Plant Allergenic Extract
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 68703-0315-30 (68703031530)

    NDC Package Code 68703-315-30
    Billing NDC 68703031530
    Package 180 TABLET in 1 BOTTLE, GLASS (68703-315-30)
    Marketing Start Date 2018-12-17
    NDC Exclude Flag N
    Pricing Information N/A