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    NDC 00067-6094-01 Theraflu 650; 20; 10 mg/1; mg/1; mg/1 Details

    Theraflu 650; 20; 10 mg/1; mg/1; mg/1

    Theraflu 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; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00067-6094
    Product ID 0067-6094_37cc655c-2189-46f0-9265-184c94e3c327
    Associated GPIs 43996903406330
    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
    Proprietary Name Suffix PowerPods Daytime Severe Cold
    Non-Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN, PHENYLEPHRINE
    Product Type HUMAN OTC DRUG
    Dosage Form POWDER, FOR SOLUTION
    Route ORAL
    Active Ingredient Strength 650; 20; 10
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH DRUG
    Application Number M012
    Listing Certified Through 2024-12-31

    Package

    NDC 00067-6094-01 (00067609401)

    NDC Package Code 0067-6094-01
    Billing NDC 00067609401
    Package 8 POUCH in 1 CARTON (0067-6094-01) / 1 POWDER, FOR SOLUTION in 1 POUCH (0067-6094-02)
    Marketing Start Date 2018-07-28
    NDC Exclude Flag N
    Pricing Information N/A