Label: PRO-TECT HOT SPOT SKIN MEDICATION- benzalkonium chloride liquid

  • NDC Code(s): 62001-0317-1
  • Packager: Straight Arrow Products, Inc.
  • Category: OTC ANIMAL DRUG LABEL

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Drug Label Information

Updated July 6, 2023

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  • Active Ingredient:

      Benzalkonium chloride

  • Purpose:

    Purpose:  Pro-Tect Hot Spot Medication for dogs is formulated to be effective for the treatment of skin inflammations.  Specifically kills  staphylococcus intermedius; bacteria most commonly associated with "Hot Spots" on dogs.  Also, treats dogs for the secondary skin infections caused by viral, fungal or bacterial organisms.  Pro-Tect Hot Spot is an effective first aid treatment for superficial cuts, scrapes, and abrasions.  Best of all, Pro-Tect Hot Spot contains no alcohol and is a non-stinging formula.

    Symptons of Hot Spots:  Hot Spots are usually accompanied by incessant rubbing, scratching, and biting due to intense itching.  Other signs are moist reddened areas, hair loss, and flaky skin.  Hot spots are usually warm to the touch.

  • Directions for Use:

    Trim the hair around the sore.  Wash the area with mild soap and water, rinse and pat dry.  Apply Pro-Tect Hot Spot to affected area.  Does not require dabbing on with a cotton ball.  Do not use on puppies under 6 weeks of age.

  • General Precautions:

      Consult a veterinarian if any problems persist or are of concern. 

    Caution:  KEEP OUT OF REACH OF CHILDREN

  • PRINCIPAL DISPLAY PANEL

    Pro-Tect AM Hot Spot LabelPro-Tect AM Hot Spot LabelPro-Tect AM Hot Spot Label

  • INGREDIENTS AND APPEARANCE
    PRO-TECT HOT SPOT SKIN MEDICATION 
    benzalkonium chloride liquid
    Product Information
    Product TypeOTC ANIMAL DRUGItem Code (Source)NDC:62001-0317
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE.001 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    WATER (UNII: 059QF0KO0R)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    COCAMIDOPROPYL BETAINE (UNII: 5OCF3O11KX)  
    HYPROMELLOSES (UNII: 3NXW29V3WO)  
    CETRIMONIUM CHLORIDE (UNII: UC9PE95IBP)  
    IMIDUREA (UNII: M629807ATL)  
    DIDECYLDIMONIUM CHLORIDE (UNII: JXN40O9Y9B)  
    OCTOXYNOL 9 (UNII: 7JPC6Y25QS)  
    QUATERNIUM-15 (UNII: E40U03LEM0)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    ANHYDROUS CITRIC ACID (UNII: XF417D3PSL)  
    ALLANTOIN (UNII: 344S277G0Z)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    D&C GREEN NO. 5 (UNII: 8J6RDU8L9X)  
    TROLAMINE (UNII: 9O3K93S3TK)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:62001-0317-1118 g in 1 BOTTLE, PLASTIC
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    unapproved drug other09/25/2003
    Labeler - Straight Arrow Products, Inc. (061580593)
    Registrant - Straight Arrow Products, Inc. (061580593)
    Establishment
    NameAddressID/FEIBusiness Operations
    Straight Arrow Products, Inc.052165154manufacture, pack
    Establishment
    NameAddressID/FEIBusiness Operations
    Lonza Biologics, Inc.093149750api manufacture