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    NDC 30142-0109-30 Mucus Relief DM 20; 400 mg/1; mg/1 Details

    Mucus Relief DM 20; 400 mg/1; mg/1

    Mucus Relief DM is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by The Kroger Co.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN.

    Product Information

    NDC 30142-0109
    Product ID 30142-109_aaf8eb37-aba5-41b1-b472-bd8598b9110e
    Associated GPIs
    GCN Sequence Number 058386
    GCN Sequence Number Description guaifenesin/dextromethorphan TABLET 400MG-20MG ORAL
    HIC3 B3T
    HIC3 Description NON-OPIOID ANTITUSSIVE AND EXPECTORANT COMBINATION
    GCN 23807
    HICL Sequence Number 000223
    HICL Sequence Number Description GUAIFENESIN/DEXTROMETHORPHAN HBR
    Brand/Generic Generic
    Proprietary Name Mucus Relief DM
    Proprietary Name Suffix n/a
    Non-Proprietary Name Dextromethorphan Hydrobromide and Guaifenesin
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 20; 400
    Active Ingredient Units mg/1; mg/1
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN
    Labeler Name The Kroger Co.
    Pharmaceutical Class Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through n/a

    Package

    NDC 30142-0109-30 (30142010930)

    NDC Package Code 30142-109-30
    Billing NDC 30142010930
    Package 1 BOTTLE in 1 BOX (30142-109-30) / 30 TABLET, COATED in 1 BOTTLE
    Marketing Start Date 2010-01-02
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL e99e4e92-c42b-4c05-a598-dd81eca23593 Details

    Revised: 11/2021