Label: UDDER BALM- oxyquinoline ointment

  • NDC Code(s): 15878-413-13, 15878-413-18
  • Packager: H. W. Naylor Company Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated January 4, 2013

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  • Active Ingredients

    8-Hydroxyquinoline .14%

  • Purpose

    Chapped teats, Minor cuts, scrapes, scratches, chafes, windburn, sunburn.

  • Directions

    Apply liberally after each milking or as often as necessary.

  • Safety

    CAUTION: Do not use in case of deep puncture wounds or serious burns – consult veterinarian.

    If redness, irritation or swelling persists or increases, discontinue use and consult veterinarian.

    Thoroughly wash udder and teats before milking.

    Animal Use Only

  • KEEP FROM REACH OF CHILDREN

  • Other Ingredients

    Petrolatum, Water, Lanolin, Wax, Oil of Clove, Sodium Borate, Color, Isopropyl Alcohol .2%.

  • Questions?

    H. W. NAYLOR CO., INC.
    MORRIS, NY 13808 U.S.A.

  • Principal Display Panel

    Dr. Naylor®

    UDDER BALM

    NET WT. 9 OZ. (255 GRAMS)

    H.W. NAYLOR CO., INC.
    MORRIS, NY  13808 U.S.A.

    ANTISEPTIC OINTMENT FOR UDDER AND TEATS

    Designed to remain in prolonged antiseptic contact, to reduce danger of external infection by inhibiting bacterial growth, and permit clean natural healing.

    UDDER MASSAGE: To promote better circulation in congested udder, apply liberally with thorough massage, removing milk at each application.

    Expiration date on underside of can.

    Made in U.S.A.

    Spec 6016

    Label
  • INGREDIENTS AND APPEARANCE
    UDDER BALM  
    oxyquinoline ointment
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:15878-413
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    Oxyquinoline (UNII: 5UTX5635HP) (Oxyquinoline - UNII:5UTX5635HP) Oxyquinoline.25 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    Petrolatum (UNII: 4T6H12BN9U)  
    Water (UNII: 059QF0KO0R)  
    Lanolin (UNII: 7EV65EAW6H)  
    Yellow Wax (UNII: 2ZA36H0S2V)  
    Paraffin (UNII: I9O0E3H2ZE)  
    Clove Leaf Oil (UNII: VCA5491KVF)  
    Sodium Borate (UNII: 91MBZ8H3QO)  
    Apocarotenal (UNII: V22N3E2U32)  
    .beta.-carotene (UNII: 01YAE03M7J)  
    Isopropyl Alcohol (UNII: ND2M416302)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:15878-413-13255 g in 1 CAN
    2NDC:15878-413-181200 g in 1 CAN
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other01/01/1964
    Labeler - H. W. Naylor Company Inc. (002080190)
    Establishment
    NameAddressID/FEIBusiness Operations
    H. W. Naylor Company Inc.002080190API MANUFACTURE, MANUFACTURE
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Safety

Report Adverse Events (Animal Drug), FDA Safety Recalls (Animal Drug)

Related Resources

Clinical Trials, PubMed, Biochemical Data Summary

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