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    NDC 69396-0135-25 Triple Antibiotic 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g Details

    Triple Antibiotic 400; 3.5; 5000 [USP'U]/g; mg/g; [USP'U]/g

    Triple Antibiotic is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by Trifecta Pharmaceuticals USA LLC. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE.

    Product Information

    NDC 69396-0135
    Product ID 69396-135_087d58d8-6682-d72c-e063-6294a90a068e
    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, Polymyxin B Sulfate
    Product Type HUMAN OTC DRUG
    Dosage Form OINTMENT
    Route TOPICAL
    Active Ingredient Strength 400; 3.5; 5000
    Active Ingredient Units [USP'U]/g; mg/g; [USP'U]/g
    Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE
    Labeler Name Trifecta Pharmaceuticals USA LLC
    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 M004
    Listing Certified Through 2024-12-31

    Package

    NDC 69396-0135-25 (69396013525)

    NDC Package Code 69396-135-25
    Billing NDC 69396013525
    Package 25 PACKET in 1 CARTON (69396-135-25) / .9 g in 1 PACKET
    Marketing Start Date 2023-10-23
    NDC Exclude Flag N
    Pricing Information N/A