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    NDC 41250-0137-06 Mucus Relief 20; 400; 10 mg/20mL; mg/20mL; mg/20mL Details

    Mucus Relief 20; 400; 10 mg/20mL; mg/20mL; mg/20mL

    Mucus Relief is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by MEIJER, INC.. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 41250-0137
    Product ID 41250-137_f6b45447-1204-4f11-8963-af22e5030db4
    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 Mucus Relief
    Proprietary Name Suffix Severe Congestion and Cough
    Non-Proprietary Name Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 20; 400; 10
    Active Ingredient Units mg/20mL; mg/20mL; mg/20mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name MEIJER, INC.
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], 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
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through n/a

    Package

    NDC 41250-0137-06 (41250013706)

    NDC Package Code 41250-137-06
    Billing NDC 41250013706
    Package 177 mL in 1 BOTTLE, PLASTIC (41250-137-06)
    Marketing Start Date 2015-02-28
    NDC Exclude Flag N
    Pricing Information N/A