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    NDC 00363-0782-06 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 Walgreens. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00363-0782
    Product ID 0363-0782_7cfaed4f-8f79-4507-b44c-d92f51119173
    Associated GPIs 43993002687420
    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 Maximum StrengthCold Flu and Sore Throat
    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 Walgreens
    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 00363-0782-06 (00363078206)

    NDC Package Code 0363-0782-06
    Billing NDC 00363078206
    Package 177 mL in 1 BOTTLE, PLASTIC (0363-0782-06)
    Marketing Start Date 2017-05-31
    NDC Exclude Flag N
    Pricing Information N/A