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    NDC 50580-0515-02 TYLENOL Cold Max 325; 10; 5 mg/1; mg/1; mg/1 Details

    TYLENOL Cold Max 325; 10; 5 mg/1; mg/1; mg/1

    TYLENOL Cold Max is a ORAL TABLET, FILM COATED in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 50580-0515
    Product ID 50580-515_0e1afc73-2bcb-12f9-e063-6294a90a1573
    Associated GPIs
    GCN Sequence Number 060981
    GCN Sequence Number Description d-methorphan/PE/acetaminophen TABLET 10-5-325MG ORAL
    HIC3 B4M
    HIC3 Description NON-OPIOID ANTITUSSIVE-DECONGESTANT-ANALGESIC COMB
    GCN 27135
    HICL Sequence Number 008885
    HICL Sequence Number Description DEXTROMETHORPHAN HBR/PHENYLEPHRINE HCL/ACETAMINOPHEN
    Brand/Generic Generic
    Proprietary Name TYLENOL Cold Max
    Proprietary Name Suffix Day
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, and phenylephrine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, FILM COATED
    Route ORAL
    Active Ingredient Strength 325; 10; 5
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name Johnson & Johnson Consumer Inc.
    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 n/a

    Package

    NDC 50580-0515-02 (50580051502)

    NDC Package Code 50580-515-02
    Billing NDC 50580051502
    Package 2 BLISTER PACK in 1 CARTON (50580-515-02) / 12 TABLET, FILM COATED in 1 BLISTER PACK
    Marketing Start Date 2018-12-21
    NDC Exclude Flag N
    Pricing Information N/A