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    NDC 59779-0671-16 Night Time Cold and Flu Relief 325; 15; 6.25 mg/1; mg/1; mg/1 Details

    Night Time Cold and Flu Relief 325; 15; 6.25 mg/1; mg/1; mg/1

    Night Time Cold and Flu Relief is a ORAL CAPSULE, LIQUID FILLED in the HUMAN OTC DRUG category. It is labeled and distributed by CVS Pharmacy. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE.

    Product Information

    NDC 59779-0671
    Product ID 59779-671_53e93a2c-8d91-4d94-80b0-276ea226d7ce
    Associated GPIs 43998903350120
    GCN Sequence Number 059455
    GCN Sequence Number Description DM/acetaminophen/doxylamine CAPSULE 15MG-325MG ORAL
    HIC3 B4G
    HIC3 Description NON-OPIOID ANTITUS-1ST GEN ANTIHIST-ANALGESIC COMB
    GCN 25094
    HICL Sequence Number 025663
    HICL Sequence Number Description DEXTROMETHORPHAN HBR/ACETAMINOPHEN/DOXYLAMINE
    Brand/Generic Generic
    Proprietary Name Night Time Cold and Flu Relief
    Proprietary Name Suffix Multi Symptom
    Non-Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, DOXYLAMINE SUCCINATE
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 325; 15; 6.25
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE
    Labeler Name CVS Pharmacy
    Pharmaceutical Class 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 n/a

    Package

    NDC 59779-0671-16 (59779067116)

    NDC Package Code 59779-671-16
    Billing NDC 59779067116
    Package 16 BLISTER PACK in 1 CARTON (59779-671-16) / 1 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    Marketing Start Date 2015-09-30
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 038d3b9b-9c92-426f-a7f3-6f9861f4e293 Details

    Revised: 10/2021