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    NDC 00363-0763-40 Severe Cold and Flu 650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL Details

    Severe Cold and Flu 650; 20; 12.5; 10 mg/30mL; mg/30mL; mg/30mL; mg/30mL

    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; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00363-0763
    Product ID 0363-0763_0f9765e1-29b5-4fd5-8d23-c6ca2933c9ac
    Associated GPIs 43995904180920
    GCN Sequence Number 061342
    GCN Sequence Number Description DM/PE/acetaminophen/doxylamine LIQUID 5-325MG/15 ORAL
    HIC3 B3P
    HIC3 Description NON-OPIOID ANTITUS-1STGEN ANTIHIST-DECON-ANALGESIC
    GCN 97134
    HICL Sequence Number 033966
    HICL Sequence Number Description DEXTROMETHORPHAN HBR/PHENYLEPHRINE/ACETAMINOPHEN/DOXYLAMINE
    Brand/Generic Generic
    Proprietary Name Severe Cold and Flu
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen, Dextromethorphan HBr, Doxylamine Succinate, Phenylephrine HCl
    Product Type HUMAN OTC DRUG
    Dosage Form SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 20; 12.5; 10
    Active Ingredient Units mg/30mL; mg/30mL; mg/30mL; mg/30mL
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; DOXYLAMINE SUCCINATE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Walgreen Company
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Antihistamine [EPC], Histamine Receptor Antagonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 00363-0763-40 (00363076340)

    NDC Package Code 0363-0763-40
    Billing NDC 00363076340
    Package 355 mL in 1 BOTTLE (0363-0763-40)
    Marketing Start Date 2013-11-21
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 02f3e739-3153-412f-b2cd-6f01dcd5875b Details

    Revised: 5/2022