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    NDC 37808-0606-40 Nighttime 650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL Details

    Nighttime 650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL

    Nighttime is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by H E B. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 37808-0606
    Product ID 37808-606_6b58c344-b53f-4f9a-bb62-a85afa118079
    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 Nighttime
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, phenylephrine hydrochloride
    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 H E B
    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 37808-0606-40 (37808060640)

    NDC Package Code 37808-606-40
    Billing NDC 37808060640
    Package 355 mL in 1 BOTTLE (37808-606-40)
    Marketing Start Date 2020-03-30
    NDC Exclude Flag N
    Pricing Information N/A