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    NDC 00280-0024-01 Alka-Seltzer Plus Severe Cold PowerFast Fizz Non Drowsy 325; 10; 7.8 mg/1; mg/1; mg/1 Details

    Alka-Seltzer Plus Severe Cold PowerFast Fizz Non Drowsy 325; 10; 7.8 mg/1; mg/1; mg/1

    Alka-Seltzer Plus Severe Cold PowerFast Fizz Non Drowsy is a ORAL TABLET, EFFERVESCENT in the HUMAN OTC DRUG category. It is labeled and distributed by Bayer HealthCare LLC.. The primary component is ASPIRIN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE BITARTRATE.

    Product Information

    NDC 00280-0024
    Product ID 0280-0024_0c3debc9-8f1b-684a-e063-6394a90a5067
    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 Severe Cold PowerFast Fizz Non Drowsy
    Proprietary Name Suffix n/a
    Non-Proprietary Name asprin, dextromethorphan hydrobromide, phenylephrine bitartrate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EFFERVESCENT
    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 Bayer HealthCare LLC.
    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 00280-0024-01 (00280002401)

    NDC Package Code 0280-0024-01
    Billing NDC 00280002401
    Package 10 POUCH in 1 CARTON (0280-0024-01) / 2 TABLET, EFFERVESCENT in 1 POUCH
    Marketing Start Date 2020-04-30
    NDC Exclude Flag N
    Pricing Information N/A
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