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    NDC 69842-0565-26 Severe Tussin CF 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL Details

    Severe Tussin CF 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL

    Severe Tussin CF 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 69842-0565
    Product ID 69842-565_c1cae744-6b76-4a96-b40c-599b0fd28049
    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 Tussin CF
    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 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 CVS Pharmacy
    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 2024-12-31

    Package

    NDC 69842-0565-26 (69842056526)

    NDC Package Code 69842-565-26
    Billing NDC 69842056526
    Package 1 BOTTLE in 1 CARTON (69842-565-26) / 118 mL in 1 BOTTLE
    Marketing Start Date 2018-06-25
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL ede1f6a7-0aec-4bc0-aad8-d12a2369d9b7 Details

    Revised: 11/2019