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    NDC 00067-0103-06 Theraflu Severe Cold Relief Daytime Honey Ginger 650; 20 mg/1; mg/1 Details

    Theraflu Severe Cold Relief Daytime Honey Ginger 650; 20 mg/1; mg/1

    Theraflu Severe Cold Relief Daytime Honey Ginger is a ORAL POWDER, FOR SOLUTION 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.

    Product Information

    NDC 00067-0103
    Product ID 0067-0103_0bdc6458-3976-85a4-e063-6394a90a5d41
    Associated GPIs
    GCN Sequence Number n/a
    GCN Sequence Number Description n/a
    HIC3 n/a
    HIC3 Description n/a
    GCN n/a
    HICL Sequence Number n/a
    HICL Sequence Number Description n/a
    Brand/Generic n/a
    Proprietary Name Theraflu Severe Cold Relief Daytime Honey Ginger
    Proprietary Name Suffix n/a
    Non-Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN HBr
    Product Type HUMAN OTC DRUG
    Dosage Form POWDER, FOR SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 20
    Active Ingredient Units mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class 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 DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 00067-0103-06 (00067010306)

    NDC Package Code 0067-0103-06
    Billing NDC 00067010306
    Package 6 PACKET in 1 CARTON (0067-0103-06) / 1 POWDER, FOR SOLUTION in 1 PACKET
    Marketing Start Date 2023-12-01
    NDC Exclude Flag N
    Pricing Information N/A
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