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    NDC 63824-0261-66 Mucinex Sinus-Max 650; 400; 10 mg/20mL; mg/20mL; mg/20mL Details

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

    Mucinex Sinus-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; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 63824-0261
    Product ID 63824-261_043ea5d8-085e-3a4a-e063-6394a90add46
    Associated GPIs 43996703500930
    GCN Sequence Number 067923
    GCN Sequence Number Description guaifen/phenyleph/acetaminophn LIQUID 10-650/20 ORAL
    HIC3 B3N
    HIC3 Description DECONGESTANT-ANALGESIC-EXPECTORANT COMBINATION
    GCN 30574
    HICL Sequence Number 023719
    HICL Sequence Number Description GUAIFENESIN/PHENYLEPHRINE HCL/ACETAMINOPHEN
    Brand/Generic Brand
    Proprietary Name Mucinex Sinus-Max
    Proprietary Name Suffix Severe Congestion Relief
    Non-Proprietary Name ACETAMINOPHEN, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 400; 10
    Active Ingredient Units mg/20mL; mg/20mL; mg/20mL
    Substance Name ACETAMINOPHEN; 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], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through n/a

    Package

    NDC 63824-0261-66 (63824026166)

    NDC Package Code 63824-261-66
    Billing NDC 63824026166
    Package 180 mL in 1 BOTTLE (63824-261-66)
    Marketing Start Date 2014-03-26
    NDC Exclude Flag N
    Pricing Information N/A