Label: OINKMENT- ethyl alcohol, sodium propionate liquid

  • NDC Code(s): 57932-005-01
  • Packager: Animal Science Products, Inc.
  • Category: OTC ANIMAL DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: unapproved drug other

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Drug Label Information

Updated November 18, 2024

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  • Active Ingredient

    Ethyl Alcohol.......................................72.6%

    Sodium Propionate...............................0.5%

  • Purpose

    QUICK-DRYING ANTIMICROBIAL FLEXIBLE FILM BANDAGE

    FOR VETERINARY USE ONLY

  • Uses

    For use as a topical microbiocidal barrier on the skin of swine to shield from abrasion and guard against contamination that may cause infection

  • Warnings

    • For external use only.
    • Store at room temperature.
    • Not for human use.
    • Keep out of reach of children.
  • Directions

    Shake well before use. For best results, clean and dry the wound and surrounding skin for good adhesion. Apply Oinkment with spray tip 6 inches from wound, spraying to completely cover the wound and overlap onto surrounding healthy skin.

    Reapply every other day or as required to keep the wound sealed until satisfactory.

  • ADVANTAGES


    • Easy to spray, dries fast to form a flexible film bandage for abrasions, cuts and scrapes
    • Covers and seals wound to maintain clean, moist healing environment
    • Antibacterial and antifungal activity
    • Deters tail biting
    • Soothing analgesic action
    • Highly visible
    • Safe, non-toxic, 100% GRAS (21 CFR) food approved components
    • No preslaughter withdrawal required
    • Removal and cleanup with water

  • Keep Out Of reach of Children

  • Inactive Ingredient

    Anhydrous citric acid, Water, FD&C yellow no. 5, FD&C blue no. 1, Methylcellulose 

  • Product label

    Bottle label

    image description

  • Product label

    Box label

    image description

  • INGREDIENTS AND APPEARANCE
    OINKMENT 
    ethyl alcohol, sodium propionate liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:57932-005
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    ALCOHOL (UNII: 3K9958V90M) (ALCOHOL - UNII:3K9958V90M) ALCOHOL7.2 mg  in 1 mL
    SODIUM PROPIONATE (UNII: DK6Y9P42IN) (PROPIONIC ACID - UNII:JHU490RVYR) SODIUM PROPIONATE0.5 mg  in 1 mL
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    METHYLCELLULOSE, UNSPECIFIED (UNII: Z944H5SN0H)  
    FD&C YELLOW NO. 5 (UNII: I753WB2F1M)  
    FD&C BLUE NO. 1 (UNII: H3R47K3TBD)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57932-005-0112 in 1 BOX
    11000 mL in 1 BOTTLE
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other05/14/2020
    Labeler - Animal Science Products, Inc. (151824091)
    Establishment
    NameAddressID/FEIBusiness Operations
    Animal Science Products Inc.151824091manufacture
    Establishment
    NameAddressID/FEIBusiness Operations
    Delta Synthetic Co., Ltd.656128618api manufacture
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