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    NDC 36800-0035-06 MUCUS RELIEF 650; 400; 10 mg/20mL; mg/20mL; mg/20mL Details

    MUCUS RELIEF 650; 400; 10 mg/20mL; mg/20mL; mg/20mL

    MUCUS RELIEF is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by TOP CARE (Topco Associates LLC). The primary component is ACETAMINOPHEN; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 36800-0035
    Product ID 36800-035_c89137a7-f348-4860-8106-c21adbf3d7bf
    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 MUCUS RELIEF
    Proprietary Name Suffix Cold and Sinus Maximum Strength
    Non-Proprietary Name Acetaminophen, Guaifenesin, Phenylephrine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    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 TOP CARE (Topco Associates 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 DRUG
    Application Number M012
    Listing Certified Through n/a

    Package

    NDC 36800-0035-06 (36800003506)

    NDC Package Code 36800-035-06
    Billing NDC 36800003506
    Package 177 mL in 1 BOTTLE, PLASTIC (36800-035-06)
    Marketing Start Date 2015-11-30
    NDC Exclude Flag N
    Pricing Information N/A