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    NDC 63868-0912-01 Multi Action 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g Details

    Multi Action 500; 3.5; 10000; 10 [USP'U]/g; mg/g; [USP'U]/g; mg/g

    Multi Action is a TOPICAL OINTMENT in the HUMAN OTC DRUG category. It is labeled and distributed by Chain Drug Marketing Association Inc.. The primary component is BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE.

    Product Information

    NDC 63868-0912
    Product ID 63868-912_fc61822a-3fba-343c-e053-6294a90af72c
    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 Multi Action
    Proprietary Name Suffix n/a
    Non-Proprietary Name Bacitracinzinc,NeomycinSulfate,PolymyxinBSulfate,PramoxineHCL
    Product Type HUMAN OTC DRUG
    Dosage Form OINTMENT
    Route TOPICAL
    Active Ingredient Strength 500; 3.5; 10000; 10
    Active Ingredient Units [USP'U]/g; mg/g; [USP'U]/g; mg/g
    Substance Name BACITRACIN ZINC; NEOMYCIN SULFATE; POLYMYXIN B SULFATE; PRAMOXINE HYDROCHLORIDE
    Labeler Name Chain Drug Marketing Association 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 63868-0912-01 (63868091201)

    NDC Package Code 63868-912-01
    Billing NDC 63868091201
    Package 1 TUBE in 1 BOX (63868-912-01) / 28.3 g in 1 TUBE
    Marketing Start Date 2022-08-31
    NDC Exclude Flag N
    Pricing Information N/A