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    NDC 71971-6030-00 Real Relief 8; 8; 8; 8; 8; 8; 8; 8 [hp_X]/1; [hp_X]/1; [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; 8; 8 [hp_X]/1; [hp_X]/1; [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 Homeolab International (Canada) inc. The primary component is ARALIA RACEMOSA ROOT; ARSENIC TRIOXIDE; COPPER; EUPHRASIA STRICTA; LOBARIA PULMONARIA; ONION; SCHOENOCAULON OFFICINALE SEED; STRYCHNOS NUX-VOMICA SEED.

    Product Information

    NDC 71971-6030
    Product ID 71971-6030_4064be78-c5a6-4b5f-9879-7092234c952f
    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 Allium cepa, Aralia racemosa, Arsenicum album, Cuprum metallicum, Euphrasia officinalis, Nux vomica, Sabadilla, Sticta pulmonaria
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 8; 8; 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; [hp_X]/1; [hp_X]/1
    Substance Name ARALIA RACEMOSA ROOT; ARSENIC TRIOXIDE; COPPER; EUPHRASIA STRICTA; LOBARIA PULMONARIA; ONION; SCHOENOCAULON OFFICINALE SEED; STRYCHNOS NUX-VOMICA SEED
    Labeler Name Homeolab International (Canada) inc
    Pharmaceutical Class Allergens [CS], Allergens [CS], Cell-mediated Immunity [PE], Cell-mediated Immunity [PE], Copper [CS], Copper-containing Intrauterine Device [EPC], Decreased Embryonic Implantation [PE], Decreased Sperm Motility [PE], Dietary Proteins [CS], Increased Hist
    DEA Schedule n/a
    Marketing Category UNAPPROVED HOMEOPATHIC
    Application Number n/a
    Listing Certified Through 2024-12-31

    Package

    NDC 71971-6030-00 (71971603000)

    NDC Package Code 71971-6030-0
    Billing NDC 71971603000
    Package 1 BOTTLE in 1 CARTON (71971-6030-0) / 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 d2459cd9-12e0-4ee4-950a-05d78023c89b Details

    Revised: 1/2020