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    NDC 72189-0361-15 LenzaPro Flex Path 40; 40 mg/g; mg/g Details

    LenzaPro Flex Path 40; 40 mg/g; mg/g

    LenzaPro Flex Path is a TOPICAL PATCH in the HUMAN OTC DRUG category. It is labeled and distributed by Direct_Rx. The primary component is LIDOCAINE; MENTHOL.

    Product Information

    NDC 72189-0361
    Product ID 72189-361_e2aab4b8-d94d-a38a-e053-2a95a90a2795
    Associated GPIs 90859902885950
    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 LenzaPro Flex Path
    Proprietary Name Suffix n/a
    Non-Proprietary Name LenzaPro Flex Path
    Product Type HUMAN OTC DRUG
    Dosage Form PATCH
    Route TOPICAL
    Active Ingredient Strength 40; 40
    Active Ingredient Units mg/g; mg/g
    Substance Name LIDOCAINE; MENTHOL
    Labeler Name Direct_Rx
    Pharmaceutical Class Amide Local Anesthetic [EPC], Amides [CS], Antiarrhythmic [EPC], Local Anesthesia [PE]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part348
    Listing Certified Through 2023-12-31

    Package

    NDC 72189-0361-15 (72189036115)

    NDC Package Code 72189-361-15
    Billing NDC 72189036115
    Package 3 g in 1 BOX (72189-361-15)
    Marketing Start Date 2022-06-22
    NDC Exclude Flag N
    Pricing Information N/A
    << 72189-0360-90 72189-0362-60 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL e20b3c53-d18c-9ddb-e053-2a95a90ad6f4 Details

    Revised: 6/2022
    Document Id: e2aab4b8-d94d-a38a-e053-2a95a90a2795
    Set id: e20b3c53-d18c-9ddb-e053-2a95a90ad6f4
    Version: 2
    Effective Time: 20220630