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    NDC 50580-0529-01 Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack Details

    Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack

    Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack is a KIT in the HUMAN OTC DRUG category. It is labeled and distributed by Johnson & Johnson Consumer Inc.. The primary component is .

    Product Information

    NDC 50580-0529
    Product ID 50580-529_f79eb306-4339-d012-e053-6394a90a77c0
    Associated GPIs
    GCN Sequence Number 071425
    GCN Sequence Number Description doxylam/PE/DM/acetaminophen/GG LIQUID SEQ 5-325MG/15 ORAL
    HIC3 B4O
    HIC3 Description NON-OPIOID ANTITUS-1ST ANTIHIST-DECON-ANALG-EXPECT
    GCN 35204
    HICL Sequence Number 040604
    HICL Sequence Number Description DOXYLAMINE/PHENYLEPHRINE/DEXTROMETHORPHAN/ACETAMINOPHEN/GG
    Brand/Generic Generic
    Proprietary Name Tylenol Cold Plus Flu Severe Day and Tylenol Cold Plus Flu Plus Cough Night 3-Pack
    Proprietary Name Suffix n/a
    Non-Proprietary Name acetaminophen, dextromethorphan hydrobromide, doxylamine succinate, and guaifenesin, phenylephrine hydrochloride
    Product Type HUMAN OTC DRUG
    Dosage Form KIT
    Route n/a
    Active Ingredient Strength n/a
    Active Ingredient Units n/a
    Substance Name n/a
    Labeler Name Johnson & Johnson Consumer Inc.
    Pharmaceutical Class n/a
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part341
    Listing Certified Through 2024-12-31

    Package

    NDC 50580-0529-01 (50580052901)

    NDC Package Code 50580-529-01
    Billing NDC 50580052901
    Package 1 KIT in 1 PACKAGE (50580-529-01) * 240 mL in 1 BOTTLE (50580-369-01) * 240 mL in 1 BOTTLE, PLASTIC (50580-403-08)
    Marketing Start Date 2019-08-05
    NDC Exclude Flag N
    Pricing Information N/A