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    NDC 53809-0250-01 DOMETUSS-G 20; 200; 10 mg/1; mg/1; mg/1 Details

    DOMETUSS-G 20; 200; 10 mg/1; mg/1; mg/1

    DOMETUSS-G is a ORAL TABLET in the HUMAN OTC DRUG category. It is labeled and distributed by DOMEL. The primary component is DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE.

    Product Information

    NDC 53809-0250
    Product ID 53809-250_dc4a9eb6-1eb6-46ed-b51d-ef80ec05e694
    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 DOMETUSS-G
    Proprietary Name Suffix n/a
    Non-Proprietary Name GUAIFENESIN, DEXTROMETHORPHAN HYDROBROMIDE, and PHENYLEPHRINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form TABLET
    Route ORAL
    Active Ingredient Strength 20; 200; 10
    Active Ingredient Units mg/1; mg/1; mg/1
    Substance Name DEXTROMETHORPHAN HYDROBROMIDE; GUAIFENESIN; PHENYLEPHRINE HYDROCHLORIDE
    Labeler Name DOMEL
    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 FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 53809-0250-01 (53809025001)

    NDC Package Code 53809-250-01
    Billing NDC 53809025001
    Package 100 TABLET in 1 BOTTLE (53809-250-01)
    Marketing Start Date 2019-11-11
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 19e06e4d-9efb-4059-a33d-4a89c3a2534c Details

    Revised: 5/2020