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    NDC 49035-0839-06 Maximum Strength Mucus Relief DM 20; 400 mg/20mL; mg/20mL Details

    Maximum Strength Mucus Relief DM 20; 400 mg/20mL; mg/20mL

    Maximum Strength Mucus Relief DM is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Wal-Mart Stores,Inc.,. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

    Product Information

    NDC 49035-0839
    Product ID 49035-839_97bacb8f-c672-40cd-9f9d-f2aced8c7283
    Associated GPIs 43997002520905
    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 Maximum Strength Mucus Relief DM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dextromethorphan hydrobromide and Guaifenesin
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 20; 400
    Active Ingredient Units mg/20mL; mg/20mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
    Labeler Name Wal-Mart Stores,Inc.,
    Pharmaceutical Class Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Ant
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 49035-0839-06 (49035083906)

    NDC Package Code 49035-839-06
    Billing NDC 49035083906
    Package 180 mL in 1 BOTTLE (49035-839-06)
    Marketing Start Date 2018-05-01
    NDC Exclude Flag N
    Pricing Information N/A