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    NDC 00113-0019-40 Good Sense Severe NightTime 650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL Details

    Good Sense Severe NightTime 650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL

    Good Sense Severe NightTime is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by L. Perrigo Company. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00113-0019
    Product ID 0113-0019_21fad873-3e4b-47ee-98d9-85f964bb9293
    Associated GPIs 43995904180920
    GCN Sequence Number 061342
    GCN Sequence Number Description DM/PE/acetaminophen/doxylamine LIQUID 5-325MG/15 ORAL
    HIC3 B3P
    HIC3 Description NON-OPIOID ANTITUS-1STGEN ANTIHIST-DECON-ANALGESIC
    GCN 97134
    HICL Sequence Number 033966
    HICL Sequence Number Description DEXTROMETHORPHAN HBR/PHENYLEPHRINE/ACETAMINOPHEN/DOXYLAMINE
    Brand/Generic Generic
    Proprietary Name Good Sense Severe NightTime
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen, dextromethorphan HBr, doxylamine succinate, phenylephrine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 20; 12.5; 10
    Active Ingredient Units mg/30mL; mg/30mL; mg/30mL; mg/30mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name L. Perrigo Company
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 00113-0019-40 (00113001940)

    NDC Package Code 0113-0019-40
    Billing NDC 00113001940
    Package 354 mL in 1 BOTTLE (0113-0019-40)
    Marketing Start Date 2015-11-24
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 0e3c36c9-d45b-41b9-891d-a42d854295f9 Details

    Revised: 4/2022