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    NDC 69396-0132-01 Triple Antibiotic and Pain Relief 500; 3.5; 10000; 10 [USP'U]/100g; mg/100g; [USP'U]/100g; mg/100g Details

    Triple Antibiotic and Pain Relief 500; 3.5; 10000; 10 [USP'U]/100g; mg/100g; [USP'U]/100g; mg/100g

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

    Product Information

    NDC 69396-0132
    Product ID 69396-132_0bf08cf6-be40-f9aa-e063-6294a90a4393
    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 and Pain Relief
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bacitracin,Neomycin,PolymyxinB,Pramoxine
    Product Type HUMAN OTC DRUG
    Dosage Form OINTMENT
    Route TOPICAL
    Active Ingredient Strength 500; 3.5; 10000; 10
    Active Ingredient Units [USP'U]/100g; mg/100g; [USP'U]/100g; mg/100g
    Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
    Labeler Name Trifecta Pharmaceutical 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 69396-0132-01 (69396013201)

    NDC Package Code 69396-132-01
    Billing NDC 69396013201
    Package 1 TUBE in 1 BOX (69396-132-01) / 28.3 g in 1 TUBE
    Marketing Start Date 2023-12-07
    NDC Exclude Flag N
    Pricing Information N/A