Search by Drug Name or NDC

    NDC 00363-0603-40 Severe Cold and Flu 325; 10; 200; 5 mg/15mL; mg/15mL; mg/15mL; mg/15mL Details

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

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

    Product Information

    NDC 00363-0603
    Product ID 0363-0603_5775e31a-1333-4f37-9a95-0b1f4c4281a2
    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 Severe 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 Walgreen 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 00363-0603-40 (00363060340)

    NDC Package Code 0363-0603-40
    Billing NDC 00363060340
    Package 355 mL in 1 BOTTLE (0363-0603-40)
    Marketing Start Date 2013-11-21
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 54254b61-7861-4eeb-bd3c-54fd5266f4a7 Details

    Revised: 7/2022