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    NDC 00067-6801-02 Theraflu Severe Cold relief Nighttime 500; 25; 10 mg/1; mg/1; mg/1 Details

    Theraflu Severe Cold relief Nighttime 500; 25; 10 mg/1; mg/1; mg/1

    Theraflu Severe Cold relief Nighttime is a ORAL POWDER in the HUMAN OTC DRUG category. It is labeled and distributed by GlaxoSmithKline Consumer Healthcare Holdings (US) LLC. The primary component is ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 00067-6801
    Product ID 0067-6801_0d3b1bea-e2ca-4e07-8ae5-60627d230c96
    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 Nighttime
    Proprietary Name Suffix n/a
    Non-Proprietary Name Acetaminophen, Diphenhydramine Hydrochloride, Phenylephrine Hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form POWDER
    Route ORAL
    Active Ingredient Strength 500; 25; 10
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DIPHENHYDRAMINE HYDROCHLORIDE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name GlaxoSmithKline Consumer Healthcare Holdings (US) LLC
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], alpha-1 Adrenergic Agonist [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 00067-6801-02 (00067680102)

    NDC Package Code 0067-6801-02
    Billing NDC 00067680102
    Package 6 POWDER in 1 CARTON (0067-6801-02)
    Marketing Start Date 2022-01-20
    NDC Exclude Flag N
    Pricing Information N/A