Search by Drug Name or NDC

    NDC 70188-0005-04 Derma Numb Pain Relief 40 mg/g Details

    Derma Numb Pain Relief 40 mg/g

    Derma Numb Pain Relief is a TOPICAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by A.T.S. Laboratories, LLC. The primary component is LIDOCAINE HYDROCHLORIDE.

    Product Information

    NDC 70188-0005
    Product ID 70188-005_f13b322e-28cf-42e1-a2c8-fa78be44c236
    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 Derma Numb Pain Relief
    Proprietary Name Suffix n/a
    Non-Proprietary Name Lidocaine HCL
    Product Type HUMAN OTC DRUG
    Dosage Form GEL
    Route TOPICAL
    Active Ingredient Strength 40
    Active Ingredient Units mg/g
    Substance Name LIDOCAINE HYDROCHLORIDE
    Labeler Name A.T.S. Laboratories, LLC
    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 2024-12-31

    Package

    NDC 70188-0005-04 (70188000504)

    NDC Package Code 70188-005-04
    Billing NDC 70188000504
    Package 113 g in 1 PACKAGE (70188-005-04)
    Marketing Start Date 2015-07-01
    NDC Exclude Flag N
    Pricing Information N/A
    << 70188-0005-01 70188-0006-01 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 710991ae-8f82-4893-93a7-0ef3f815d132 Details

    Revised: 1/2022
    Document Id: f13b322e-28cf-42e1-a2c8-fa78be44c236
    Set id: 710991ae-8f82-4893-93a7-0ef3f815d132
    Version: 3
    Effective Time: 20220114