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    NDC 36800-0411-04 Night Time Cold and Flu Severe 325; 10; 6.25; 5 mg/1; mg/1; mg/1; mg/1 Details

    Night Time Cold and Flu Severe 325; 10; 6.25; 5 mg/1; mg/1; mg/1; mg/1

    Night Time Cold and Flu Severe is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by Topco Associates LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 36800-0411
    Product ID 36800-411_68ed6816-939a-4778-80e9-fff788e45a23
    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 Night Time Cold and Flu Severe
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen, Dextromethorphan hydrobromide, Doxylamine succinate, Phenylephrine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 325; 10; 6.25; 5
    Active Ingredient Units mg/1; mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Topco Associates LLC
    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 36800-0411-04 (36800041104)

    NDC Package Code 36800-411-04
    Billing NDC 36800041104
    Package 2 BLISTER PACK in 1 CARTON (36800-411-04) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    Marketing Start Date 2016-06-02
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9f5f051f-a464-436f-9d43-e23c48a505bc Details

    Revised: 11/2019