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    NDC 50580-0511-01 TYLENOL Cold Plus Mucus Severe 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL Details

    TYLENOL Cold Plus Mucus Severe 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL

    TYLENOL Cold Plus Mucus Severe is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 50580-0511
    Product ID 50580-511_f79e03df-d703-e23b-e053-6294a90a02ab
    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 TYLENOL Cold Plus Mucus Severe
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen, Dextromethorphan Hydrobromide, Guaifenesin, and Phenylephrine hydrochloride
    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 Johnson & Johnson Consumer Inc.
    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 50580-0511-01 (50580051101)

    NDC Package Code 50580-511-01
    Billing NDC 50580051101
    Package 240 mL in 1 BOTTLE, PLASTIC (50580-511-01)
    Marketing Start Date 2015-06-22
    NDC Exclude Flag N
    Pricing Information N/A