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    NDC 63868-0461-12 DayTime Maximum Strength Cold and Flu 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 Details

    DayTime Maximum Strength Cold and Flu 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1

    DayTime Maximum Strength 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; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 63868-0461
    Product ID 63868-461_0d748c2e-202b-4bfa-8108-eabb1717e772
    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 DayTime Maximum Strength Cold and Flu
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form CAPSULE, LIQUID FILLED
    Route ORAL
    Active Ingredient Strength 325; 10; 200; 5
    Active Ingredient Units mg/1; mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Chain Drug Marketing Association Inc.
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 63868-0461-12 (63868046112)

    NDC Package Code 63868-461-12
    Billing NDC 63868046112
    Package 1 BLISTER PACK in 1 CARTON (63868-461-12) / 12 CAPSULE, LIQUID FILLED in 1 BLISTER PACK
    Marketing Start Date 2016-08-03
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 654bbc72-ba36-4ad5-8b4b-518dac7eda19 Details

    Revised: 12/2019