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    NDC 71992-0154-20 ALKA SELTZER PLUS Cold Day and Night Effervescent 325; 10; 7.8 mg/1; mg/1; mg/1 Details

    ALKA SELTZER PLUS Cold Day and Night Effervescent 325; 10; 7.8 mg/1; mg/1; mg/1

    ALKA SELTZER PLUS Cold Day and Night Effervescent is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by Sincronia Logistica, S.A. de C.V.. The primary component is ASPIRIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE BITARTRATE.

    Product Information

    NDC 71992-0154
    Product ID 71992-154_086318bd-5067-477e-e063-6294a90ab2dd
    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 ALKA SELTZER PLUS Cold Day and Night Effervescent
    Proprietary Name Suffix n/a
    Non-Proprietary Name ASPIRIN, DEXTROMETHORPHAN HYDROBROMIDE, PHENYLEPHRINE BITARTRATE
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 325; 10; 7.8
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ASPIRIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE BITARTRATE
    Labeler Name Sincronia Logistica, S.A. de C.V.
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Anti-Inflammatory Agents, Non-Steroidal [CS], Cyclooxygenase Inhibitors [MoA], Decreased Platelet Aggregation [PE], Decreased Prostaglandin Production [PE], Nonsteroidal Anti-inflammatory Drug [EPC], Platelet Aggregation
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 71992-0154-20 (71992015420)

    NDC Package Code 71992-154-20
    Billing NDC 71992015420
    Package 20 TABLET in 1 CARTON (71992-154-20)
    Marketing Start Date 2018-07-02
    NDC Exclude Flag N
    Pricing Information N/A
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