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    NDC 00280-0020-02 Alka-Seltzer Plus Severe Cold PowerFast Fizz 325; 2; 7 mg/1; mg/1; mg/1 Details

    Alka-Seltzer Plus Severe Cold PowerFast Fizz 325; 2; 7 mg/1; mg/1; mg/1

    Alka-Seltzer Plus Severe Cold PowerFast Fizz 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; CHLORPHENIRAMINE MALEATE; PHENYLEPHRINE BITARTRATE.

    Product Information

    NDC 00280-0020
    Product ID 0280-0020_030bc78e-6d7d-06cb-e063-6394a90afa70
    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
    Proprietary Name Suffix Orange Zest
    Non-Proprietary Name aspirin, chlorpheniramine maleate, phenylephrine bitartrate
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, EFFERVESCENT
    Route ORAL
    Active Ingredient Strength 325; 2; 7
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ASPIRIN; CHLORPHENIRAMINE MALEATE; 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], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor An
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 00280-0020-02 (00280002002)

    NDC Package Code 0280-0020-02
    Billing NDC 00280002002
    Package 12 POUCH in 1 CARTON (0280-0020-02) / 2 TABLET, EFFERVESCENT in 1 POUCH
    Marketing Start Date 2023-03-30
    NDC Exclude Flag N
    Pricing Information N/A
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