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    NDC 59779-0603-40 Severe Daytime 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL Details

    Severe Daytime 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL

    Severe Daytime is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 59779-0603
    Product ID 59779-603_c34f9fa1-e11c-48c6-b868-9f2a46d6a7ef
    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 Severe Daytime
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen, dextromethorphan hbr, guaifenesin, phenylephrine hcl
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 325; 10; 200; 5
    Active Ingredient Units mg/15mL; mg/15mL; mg/15mL; mg/15mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name CVS Pharmacy
    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 59779-0603-40 (59779060340)

    NDC Package Code 59779-603-40
    Billing NDC 59779060340
    Package 355 mL in 1 BOTTLE (59779-603-40)
    Marketing Start Date 2013-12-27
    NDC Exclude Flag N
    Pricing Information N/A