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    NDC 11822-0086-01 tussin severe multi symptom cough cold plus flu CF MAX 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL Details

    tussin severe multi symptom cough cold plus flu CF MAX 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL

    tussin severe multi symptom cough cold plus flu CF MAX is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by Rite Aid Corporation. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 11822-0086
    Product ID 11822-0086_075141bb-54df-41a2-b2a0-f6484d2031e9
    Associated GPIs 66100020000305
    GCN Sequence Number 008346
    GCN Sequence Number Description ibuprofen TABLET 200 MG ORAL
    HIC3 S2B
    HIC3 Description NSAIDS, CYCLOOXYGENASE INHIBITOR TYPE ANALGESICS
    GCN 35743
    HICL Sequence Number 003723
    HICL Sequence Number Description IBUPROFEN
    Brand/Generic Generic
    Proprietary Name tussin severe multi symptom cough cold plus flu CF MAX
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen, dextromethorphan HBr, guaifenesin, phenylephrine HCl
    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 Rite Aid Corporation
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 11822-0086-01 (11822008601)

    NDC Package Code 11822-0086-1
    Billing NDC 11822008601
    Package 1 BOTTLE in 1 CARTON (11822-0086-1) / 237 mL in 1 BOTTLE
    Marketing Start Date 2017-09-22
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d3294a07-f5e6-4d77-9b90-a682265fb609 Details

    Revised: 12/2019