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    NDC 50804-0337-06 Mucus Relief Severe Congestion and Cough 20; 400; 10 mg/20mL; mg/20mL; mg/20mL Details

    Mucus Relief Severe Congestion and Cough 20; 400; 10 mg/20mL; mg/20mL; mg/20mL

    Mucus Relief Severe Congestion and Cough is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by Good Sense (Geiss, Destin & Dunn, Inc.). The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 50804-0337
    Product ID 50804-337_a59d4d8d-bd78-4a60-a765-7ff0b223db0f
    Associated GPIs 43997303100960
    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 Severe Congestion and Cough
    Proprietary Name Suffix Maximum Strength
    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 Good Sense (Geiss, Destin & Dunn, 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 DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 50804-0337-06 (50804033706)

    NDC Package Code 50804-337-06
    Billing NDC 50804033706
    Package 177 mL in 1 BOTTLE, PLASTIC (50804-337-06)
    Marketing Start Date 2016-09-30
    NDC Exclude Flag N
    Pricing Information N/A