Label: MURICIN- mupirocin ointment

  • NDC Code(s): 17033-420-15
  • Packager: Dechra Veterinary Products
  • Category: PRESCRIPTION ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: Abbreviated New Animal Drug Application

Drug Label Information

Updated December 21, 2022

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  • SPL UNCLASSIFIED SECTION

    For dermatologic use on dogs.

    CAUTION: Federal law restricts this drug to use by or on the order of a licensed veterinarian.

  • DESCRIPTION:

    Each gram of Muricin ointment contains 20 mg of mupirocin in a bland, water-washable ointment base consisting of polyethylene glycol 400 and polyethylene glycol 3350 (polyethylene glycol ointment, NF). Mupirocin is a naturally-occurring, broadspectrum antibiotic. The chemical name is (E)-(2S,3R,4R,5S)-5-[(2S,3S,4S,5S)-2,3-Epoxy-5-hydroxy-4-methylhexyl]tetrahydro-3,4-dihydroxy-β-methyl-2H-pyran-2-crotonic acid, ester with 9-hydroxynonanoic acid. The chemical structure is:

    ChemicalStructure
  • CLINICAL PHARMACOLOGY:

    Mupirocin is a chemical entity produced by fermentation of the organism Pseudomonas fluorescens. Mupirocin inhibits bacterial protein synthesis by reversibly and specifically binding to bacterial isoleucyl transfer-RNA synthetase. Due to this mode of action, mupirocin shows no cross resistance with chloramphenicol, erythromycin, gentamicin, lincomycin, neomycin, novobiocin, penicillin, streptomycin, and tetracycline. Mupirocin is an antimicrobial agent that inhibits the growth of Gram-positive and Gram-negative bacteria. Bacteria susceptible to the action of mupirocin in vitro include the aerobic isolates of Staphylococcus aureus (including methicillin-resistant strains and β-lactamase-producing strains), Staphylococcus intermedius, Staphylococcus epidermidis, other coagulase positive or negative Staphylococci, α-hemolytic Streptococci, β group A Streptococci (including S. pyogenes), other β Streptococci (including S. agalactiae), group D Streptococci (including S. faecalis and S. faecium), group Viridans Streptococci, Streptococcus pneumoniae, Corynebacterium hofmanii, Bacillus subtilis, Escherichia coli, Klebsiella pneumoniae, Proteus mirabilis, Proteus vulgaris, Enterobacter cloacae, Enterobacter aerogenes, Citrobacter freundii, Hemophilus influenzae (including β-lactamase-producing strains), Neisseria gonorrheae (including β-lactamase-producing strains), Neisseria meningitidis, Branhamella catarrhalis and Pasteurella multocida, and the anaerobic isolates of Peptostreptococcus anaerobius, Clostridium difficile, and Clostridium sporogenes.

    Clinical significance of the in vitro data is unknown except for susceptible strains of Staphylococcus aureus and Staphylococcus intermedius.

  • INDICATIONS FOR USE:

    Muricin ointment is indicated for the topical treatment of canine bacterial infections of the skin, including superficial pyoderma, caused by susceptible strains of Staphylococcus aureus and Staphylococcus intermedius.

  • CONTRAINDICATIONS:

    This drug is contraindicated in animals with a history of sensitivity reactions to any of its components.

  • WARNINGS:

     
    Because of the potential hazard of nephrotoxicity due to the polyethylene glycol content of the base, care should be exercised when using this product in treating extensive deep lesions where absorption of large quantities of polyethylene glycol is possible.
     
    Safety of use in pregnant or breeding animals has not been determined. Muricin ointment is not for ophthalmic use.
  • ADVERSE REACTIONS:

    No adverse reactions have been reported with this product. If a skin reaction such as irritation should occur, treatment should be discontinued and appropriate therapy instituted.

    To report suspected adverse drug events, for technical assistance, or to obtain a copy of the Safety Data Sheet, contact Dechra Veterinary Products at (866) 933-2472.

     
    For additional information about adverse drug experience reporting for animal drugs, contact FDA at 1-888-FDA-VETS or http://www.fda.gov/reportanimalae.
  • DOSAGE AND ADMINISTRATION:

     
    Prior to treatment, the lesion should be cleansed. Muricin ointment should be applied to the affected area twice a day. Apply a sufficient amount of ointment to completely cover the infected area. Maximum duration of treatment should not exceed 30 days.
  • HOW SUPPLIED:

     
    Muricin ointment is supplied in 15-gram tubes.

    NDC 17033-420-15.

    Store between 15° and 30°C (59° and 86°F).

    Keep out of reach of children.

    instructions
  • IMPORTANT:

    The opening of this product is covered by a metal tamper-evident seal.

    If this seal has been punctured or is not visible, do not use and return product to place of purchase.

    Approved by FDA under ANADA # 200-418

    directions

    Manufactured for:

    Dechra Veterinary Products

    Overland Park, KS 66211 USA

    Manufactured by:

    Fougera Pharmaceuticals Inc.

    Melville, NY 11747 USA

    46269504

    Rev. December 2022

  • PRINCIPAL DISPLAY PANEL - 15 g Carton

    Muricin®
    (mupirocin ointment) 2%
    For dermatologic use on dogs
    NET WT 15 g
    NDC 17033-420-15
    carton

  • INGREDIENTS AND APPEARANCE
    MURICIN 
    mupirocin ointment
    Product Information
    Product TypePRESCRIPTION ANIMAL DRUGItem Code (Source)NDC:17033-420
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MUPIROCIN (UNII: D0GX863OA5) (MUPIROCIN - UNII:D0GX863OA5) MUPIROCIN20 mg  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYETHYLENE GLYCOL 3350 (UNII: G2M7P15E5P)  
    POLYETHYLENE GLYCOL 400 (UNII: B697894SGQ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:17033-420-151 in 1 CARTON
    115 g in 1 TUBE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    ANADAANADA20041803/08/2007
    Labeler - Dechra Veterinary Products (362142734)
    Registrant - Fougera Pharmaceuticals Inc. (043838424)