Search by Drug Name or NDC

    NDC 68788-8102-02 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 Preferred Pharmaceuticals Inc.. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.

    Product Information

    NDC 68788-8102
    Product ID 68788-8102_9db15672-9009-49cb-8070-5767cd79c154
    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 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 Preferred Pharmaceuticals 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 DRUG
    Application Number 333B
    Listing Certified Through 2024-12-31

    Package

    NDC 68788-8102-02 (68788810202)

    NDC Package Code 68788-8102-2
    Billing NDC 68788810202
    Package 1 TUBE in 1 CARTON (68788-8102-2) / 28.4 g in 1 TUBE
    Marketing Start Date 2021-10-14
    NDC Exclude Flag N
    Pricing Information N/A