Search by Drug Name or NDC

    NDC 00113-0603-40 Good Sense Severe Daytime Cold and Flu 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL Details

    Good Sense Severe Daytime Cold and Flu 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL

    Good Sense Severe Daytime Cold and Flu is a ORAL SOLUTION in the HUMAN OTC DRUG category. It is labeled and distributed by L. Perrigo Company. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00113-0603
    Product ID 0113-0603_a08c5fee-fd6e-48e6-aab0-13df2043c29a
    Associated GPIs 43998304100910
    GCN Sequence Number 061341
    GCN Sequence Number Description phenylephrine/DM/acetaminop/GG LIQUID 5-325MG/15 ORAL
    HIC3 B4P
    HIC3 Description NON-OPIOID ANTITUSS-DECONGESTANT-ANALGESIC-EXPECT
    GCN 97133
    HICL Sequence Number 035445
    HICL Sequence Number Description PHENYLEPHRINE HCL/DEXTROMETHORPHAN HBR/ACETAMINOPHEN/GUAIFEN
    Brand/Generic Generic
    Proprietary Name Good Sense Severe Daytime Cold and Flu
    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 325; 10; 200; 5
    Active Ingredient Units mg/15mL; mg/15mL; mg/15mL; mg/15mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name L. Perrigo Company
    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 00113-0603-40 (00113060340)

    NDC Package Code 0113-0603-40
    Billing NDC 00113060340
    Package 354 mL in 1 BOTTLE (0113-0603-40)
    Marketing Start Date 2013-11-19
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d5faf89f-3641-4be1-8d43-35504f12fe8d Details

    Revised: 12/2021