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    NDC 58988-1170-01 Cuadriderma 500; 3.5; 10000; 10 [iU]/g; mg/g; [iU]/g; mg/g Details

    Cuadriderma 500; 3.5; 10000; 10 [iU]/g; mg/g; [iU]/g; mg/g

    Cuadriderma is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by ProMex LLC. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE.

    Product Information

    NDC 58988-1170
    Product ID 58988-1170_4d1e0271-73eb-4265-a701-33a742b81483
    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 Cuadriderma
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bacitracin Zinc, Polymyxin B Sulfate, Neomycin Sulfate, and PRAMOXINE HYDROCHLORIDE
    Product Type HUMAN OTC DRUG
    Dosage Form OINTMENT
    Route TOPICAL
    Active Ingredient Strength 500; 3.5; 10000; 10
    Active Ingredient Units [iU]/g; mg/g; [iU]/g; mg/g
    Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
    Labeler Name ProMex 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 FINAL
    Application Number part333B
    Listing Certified Through 2024-12-31

    Package

    NDC 58988-1170-01 (58988117001)

    NDC Package Code 58988-1170-1
    Billing NDC 58988117001
    Package 1 TUBE in 1 CARTON (58988-1170-1) / 28.35 g in 1 TUBE
    Marketing Start Date 2013-05-31
    NDC Exclude Flag N
    Pricing Information N/A

    Standard Product Labeling (SPL)/Prescribing Information SPL 4fa99b96-ab4b-4523-82bc-343dbaf39fb6 Details

    Revised: 1/2022