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    NDC 63868-0219-16 Nighttime Cold and Flu 325; 10; 6.25; 5 mg/1; mg/1; mg/1; mg/1 Details

    Nighttime Cold and Flu 325; 10; 6.25; 5 mg/1; mg/1; mg/1; mg/1

    Nighttime Cold and Flu is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by Chain Drug Marketing Association Inc.. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 63868-0219
    Product ID 63868-219_2f636d9f-b674-48c8-9903-89fc51187397
    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 Cold and Flu
    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 Chain Drug Marketing Association Inc.
    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 63868-0219-16 (63868021916)

    NDC Package Code 63868-219-16
    Billing NDC 63868021916
    Package 2 BLISTER PACK in 1 CARTON (63868-219-16) / 8 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    Marketing Start Date 2017-07-13
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 9022f05b-23ef-4f28-9ae8-2d0770110089 Details

    Revised: 12/2019