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    NDC 46122-0460-62 Cold Max Severe 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1 Details

    Cold Max Severe 325; 10; 200; 5 mg/1; mg/1; mg/1; mg/1

    Cold Max Severe is a ORAL TABLET, COATED in the HUMAN OTC DRUG category. It is labeled and distributed by AmeriSource Bergen. The primary component is ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 46122-0460
    Product ID 46122-460_ee2acf6a-e641-62fd-e053-2a95a90adc64
    Associated GPIs 43998304100320
    GCN Sequence Number 060553
    GCN Sequence Number Description phenylephrine/DM/acetaminop/GG TABLET 5-325-200 ORAL
    HIC3 B4P
    HIC3 Description NON-OPIOID ANTITUSS-DECONGESTANT-ANALGESIC-EXPECT
    GCN 26742
    HICL Sequence Number 035445
    HICL Sequence Number Description PHENYLEPHRINE HCL/DEXTROMETHORPHAN HBR/ACETAMINOPHEN/GUAIFEN
    Brand/Generic Generic
    Proprietary Name Cold Max Severe
    Proprietary Name Suffix n/a
    Non-Proprietary Name ACETAMINOPHEN, DEXTROMETHORPHAN HYDROBROMIDE, GUAIFENESIN, and PHENYLEPHRINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET, COATED
    Route ORAL
    Active Ingredient Strength 325; 10; 200; 5
    Active Ingredient Units mg/1; mg/1; mg/1; mg/1
    Substance Name ACETAMINOPHEN; DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name AmeriSource Bergen
    Pharmaceutical Class Adrenergic alpha1-Agonists [MoA], Decreased Respiratory Secretion Viscosity [PE], Expectorant [EPC], Increased Respiratory Secretions [PE], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through n/a

    Package

    NDC 46122-0460-62 (46122046062)

    NDC Package Code 46122-460-62
    Billing NDC 46122046062
    Package 2 BLISTER PACK in 1 CARTON (46122-460-62) / 12 TABLET, COATED in 1 BLISTER PACK
    Marketing Start Date 2018-03-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 28b3991a-fa67-48ae-ab51-908185be29c2 Details

    Revised: 11/2022