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    NDC 41163-0035-06 Mucus Relief 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL Details

    Mucus Relief 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL

    Mucus Relief is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by EQUALINE (SuperValu). The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 41163-0035
    Product ID 41163-035_0bdb7693-bb5e-4243-a24f-ddd6d3a91c86
    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 Cold Flu and Sore Throat Maximum Strength
    Non-Proprietary Name Acetaminophen, Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 650; 20; 400; 10
    Active Ingredient Units mg/20mL; mg/20mL; mg/20mL; mg/20mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name EQUALINE (SuperValu)
    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 2024-12-31

    Package

    NDC 41163-0035-06 (41163003506)

    NDC Package Code 41163-035-06
    Billing NDC 41163003506
    Package 177 mL in 1 BOTTLE, PLASTIC (41163-035-06)
    Marketing Start Date 2014-12-31
    NDC Exclude Flag N
    Pricing Information N/A