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    NDC 37808-0407-04 Mucus Multi Symptom Cold Relief 5; 100; 2.5 mg/5mL; mg/5mL; mg/5mL Details

    Mucus Multi Symptom Cold Relief 5; 100; 2.5 mg/5mL; mg/5mL; mg/5mL

    Mucus Multi Symptom Cold Relief is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by H E B. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 37808-0407
    Product ID 37808-407_52ba4afa-7ab8-42b7-b19b-73fc79484646
    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 Multi Symptom Cold Relief
    Proprietary Name Suffix Childrens
    Non-Proprietary Name Dextromethorphan HBr, Guaifenesin, Phenylephrine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 5; 100; 2.5
    Active Ingredient Units mg/5mL; mg/5mL; mg/5mL
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name H E B
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through n/a

    Package

    NDC 37808-0407-04 (37808040704)

    NDC Package Code 37808-407-04
    Billing NDC 37808040704
    Package 1 BOTTLE, PLASTIC in 1 BOX (37808-407-04) / 118 mL in 1 BOTTLE, PLASTIC
    Marketing Start Date 2016-07-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 66240ed0-8fd1-4b97-9c60-d282a0c9a19d Details

    Revised: 10/2021