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    NDC 65808-0324-01 Real Relief 8; 8; 8; 8; 8; 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1 Details

    Real Relief 8; 8; 8; 8; 8; 8 [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1

    Real Relief is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by GMP Laboratories of America, Inc.. The primary component is APIS MELLIFERA; ARNICA MONTANA; BENZOIC ACID; CAUSTICUM; COLCHICUM AUTUMNALE BULB; SODIUM CARBONATE.

    Product Information

    NDC 65808-0324
    Product ID 65808-324_b7a1ce34-a98c-22cf-e053-2a95a90afa45
    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 Real Relief
    Proprietary Name Suffix n/a
    Non-Proprietary Name Apis Mellifica, Arnica Montana, Benzoicum Acidum, Causticum, Colchicum Autumnale, Natrum Carbonicum
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 8; 8; 8; 8; 8; 8
    Active Ingredient Units [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1; [hp_X]/1
    Substance Name APIS MELLIFERA; ARNICA MONTANA; BENZOIC ACID; CAUSTICUM; COLCHICUM AUTUMNALE BULB; SODIUM CARBONATE
    Labeler Name GMP Laboratories of America, Inc.
    Pharmaceutical Class Allergens [CS], Ammonium Ion Binding Activity [MoA], Bee Venoms [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Increased IgG Production [PE], Nitrogen Binding Agent [EPC], 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 65808-0324-01 (65808032401)

    NDC Package Code 65808-324-01
    Billing NDC 65808032401
    Package 1 BOTTLE in 1 CARTON (65808-324-01) / 90 TABLET in 1 BOTTLE
    Marketing Start Date 2020-01-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL b7a1ce34-a996-22cf-e053-2a95a90afa45 Details

    Revised: 12/2020