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    NDC 00031-8751-18 Robitussin Severe Multi-Symptom Cough Cold Flu 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL Details

    Robitussin Severe Multi-Symptom Cough Cold Flu 650; 20; 400; 10 mg/20mL; mg/20mL; mg/20mL; mg/20mL

    Robitussin Severe Multi-Symptom Cough Cold Flu is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00031-8751
    Product ID 0031-8751_62ce8cd8-57d2-48a6-aaf1-d9b0cdb5753c
    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 Generic
    Proprietary Name Robitussin Severe Multi-Symptom Cough Cold Flu
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, guaifenesin, phenylephrine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    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 GlaxoSmithKline Consumer Healthcare Holdings (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 00031-8751-18 (00031875118)

    NDC Package Code 0031-8751-18
    Billing NDC 00031875118
    Package 1 BOTTLE in 1 CARTON (0031-8751-18) / 237 mL in 1 BOTTLE
    Marketing Start Date 2015-05-01
    NDC Exclude Flag N
    Pricing Information N/A