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    NDC 63824-0015-69 Mucinex Fast-Max 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL Details

    Mucinex Fast-Max 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL

    Mucinex Fast-Max is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by RB Health (US) LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 63824-0015
    Product ID 63824-015_776f2bad-f869-4274-ab93-21850fbbcd1d
    Associated GPIs 43998304100915
    GCN Sequence Number 067926
    GCN Sequence Number Description phenylephrine/DM/acetaminop/GG LIQUID 10-650/20 ORAL
    HIC3 B4P
    HIC3 Description NON-OPIOID ANTITUSS-DECONGESTANT-ANALGESIC-EXPECT
    GCN 30577
    HICL Sequence Number 035445
    HICL Sequence Number Description PHENYLEPHRINE HCL/DEXTROMETHORPHAN HBR/ACETAMINOPHEN/GUAIFEN
    Brand/Generic Brand
    Proprietary Name Mucinex Fast-Max
    Proprietary Name Suffix Cold, Flu and Sore Throat
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, and phenylephrine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 20; 400; 10
    Active Ingredient Units mg/20mL; mg/20mL; mg/20mL; mg/20mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name RB Health (US) LLC
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 63824-0015-69 (63824001569)

    NDC Package Code 63824-015-69
    Billing NDC 63824001569
    Package 266 mL in 1 BOTTLE (63824-015-69)
    Marketing Start Date 2012-02-07
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL c902b4fc-c71c-4ef2-b5cb-6c2bd019acbc Details

    Revised: 1/2022