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    NDC 51672-2120-06 Triple Antibiotic 400; 3.5; 5000 [iU]/g; mg/g; [iU]/g Details

    Triple Antibiotic 400; 3.5; 5000 [iU]/g; mg/g; [iU]/g

    Triple Antibiotic is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by Taro Pharmaceuticals U.S.A., Inc.. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.

    Product Information

    NDC 51672-2120
    Product ID 51672-2120_0d5c5ca2-8559-44b0-9319-3547eae6006d
    Associated GPIs 90109803104200
    GCN Sequence Number 007694
    GCN Sequence Number Description neomycin/bacitracin/polymyxinB OINT. (G) 3.5-400-5K TOPICAL
    HIC3 Q5W
    HIC3 Description TOPICAL ANTIBIOTICS
    GCN 85459
    HICL Sequence Number 033356
    HICL Sequence Number Description NEOMYCIN SULFATE/BACITRACIN ZINC/POLYMYXIN B
    Brand/Generic Brand
    Proprietary Name Triple Antibiotic
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bacitracin Zinc, Neomycin Sulfate, and Polymyxin B Sulfate
    Product Type HUMAN OTC DRUG
    Dosage Form OINTMENT
    Route TOPICAL
    Active Ingredient Strength 400; 3.5; 5000
    Active Ingredient Units [iU]/g; mg/g; [iU]/g
    Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
    Labeler Name Taro Pharmaceuticals U.S.A., Inc.
    Pharmaceutical Class Aminoglycoside Antibacterial [EPC], Aminoglycosides [CS], Decreased Cell Wall Synthesis & Repair [PE], Polymyxin-class Antibacterial [EPC], Polymyxins [CS]
    DEA Schedule n/a
    Marketing Category OTC MONOGRAPH FINAL
    Application Number part333B
    Listing Certified Through 2024-12-31

    Package

    NDC 51672-2120-06 (51672212006)

    NDC Package Code 51672-2120-6
    Billing NDC 51672212006
    Package 6 APPLICATOR in 1 CARTON (51672-2120-6) / .9 g in 1 APPLICATOR
    Marketing Start Date 2021-09-20
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL d77239e6-5e81-439a-b0cd-f8be59169442 Details

    Revised: 9/2021