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    NDC 10129-0070-01 Gingicaine Gel Variety Pak 200 mg/1 Details

    Gingicaine Gel Variety Pak 200 mg/1

    Gingicaine Gel Variety Pak is a DENTAL; ORAL; PERIODONTAL GEL in the HUMAN OTC DRUG category. It is labeled and distributed by Gingi-Pak a Division of the Belport. The primary component is BENZOCAINE.

    Product Information

    NDC 10129-0070
    Product ID 10129-070_62ed4ff3-18f7-5c67-e053-2991aa0a7792
    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 Gingicaine Gel Variety Pak
    Proprietary Name Suffix n/a
    Non-Proprietary Name Gingicaine Gel Variety Pak
    Product Type HUMAN OTC DRUG
    Dosage Form GEL
    Route DENTAL; ORAL; PERIODONTAL
    Active Ingredient Strength 200
    Active Ingredient Units mg/1
    Substance Name BENZOCAINE
    Labeler Name Gingi-Pak a Division of the Belport
    Pharmaceutical Class Allergens [CS], Cell-mediated Immunity [PE], Increased Histamine Release [PE], Standardized Chemical Allergen [EPC]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH NOT FINAL
    Application Number part356
    Listing Certified Through 2024-12-31

    Package

    NDC 10129-0070-01 (10129007001)

    NDC Package Code 10129-070-01
    Billing NDC 10129007001
    Package 6 GEL in 1 BOTTLE (10129-070-01)
    Marketing Start Date 2014-06-09
    NDC Exclude Flag N
    Pricing Information N/A
    << 10129-0063-05 10129-0071-01 >>

    Contents

    Standard Product Labeling (SPL)/Prescribing Information SPL 62ed4ff3-18f6-5c67-e053-2991aa0a7792 Details

    Revised: 1/2018
    Document Id: 62ed4ff3-18f7-5c67-e053-2991aa0a7792
    Set id: 62ed4ff3-18f6-5c67-e053-2991aa0a7792
    Version: 1
    Effective Time: 20180111