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    NDC 15187-0036-04 Scot-Tussin DM Maximum Strength Cough Suppressant and Cold Relief 2; 15 mg/5mL; mg/5mL Details

    Scot-Tussin DM Maximum Strength Cough Suppressant and Cold Relief 2; 15 mg/5mL; mg/5mL

    Scot-Tussin DM Maximum Strength Cough Suppressant and Cold Relief is a ORAL LIQUID in the HUMAN OTC DRUG category. It is labeled and distributed by SOCIETAL CDMO SAN DIEGO, LLC. The primary component is CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE.

    Product Information

    NDC 15187-0036
    Product ID 15187-036_de5cb377-f49b-5b4d-e053-2995a90afe3e
    Associated GPIs 43995702100925
    GCN Sequence Number 048940
    GCN Sequence Number Description chlorpheniramine/dextromethorp LIQUID 2-15MG/5ML ORAL
    HIC3 B4E
    HIC3 Description NON-OPIOID ANTITUSSIVE-1ST GEN ANTIHISTAMINE COMB.
    GCN 14924
    HICL Sequence Number 001924
    HICL Sequence Number Description CHLORPHENIRAMINE MALEATE/DEXTROMETHORPHAN HBR
    Brand/Generic Brand
    Proprietary Name Scot-Tussin DM Maximum Strength Cough Suppressant and Cold Relief
    Proprietary Name Suffix n/a
    Non-Proprietary Name chlorpheniramine maleate and dextromethorphan hydrobromide
    Product Type HUMAN OTC DRUG
    Dosage Form LIQUID
    Route ORAL
    Active Ingredient Strength 2; 15
    Active Ingredient Units mg/5mL; mg/5mL
    Substance Name CHLORPHENIRAMINE MALEATE; DEXTROMETHORPHAN HYDROBROMIDE
    Labeler Name SOCIETAL CDMO SAN DIEGO, LLC
    Pharmaceutical Class Histamine H1 Receptor Antagonists [MoA], Histamine-1 Receptor Antagonist [EPC], Sigma-1 Agonist [EPC], Sigma-1 Receptor Agonists [MoA], Uncompetitive N-methyl-D-aspartate Receptor Antagonist [EPC], Uncompetitive NMDA Receptor Antagonists [MoA]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2023-12-31

    Package

    NDC 15187-0036-04 (15187003604)

    NDC Package Code 15187-036-04
    Billing NDC 15187003604
    Package 1 BOTTLE in 1 CARTON (15187-036-04) / 118 mL in 1 BOTTLE
    Marketing Start Date 2016-01-01
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 5bbbb3f0-40bc-4dee-b352-a834a4a09908 Details

    Revised: 5/2022