PRO-TECT HOT SPOT SKIN MEDICATION- benzalkonium chloride liquid 
Straight Arrow Products, Inc.

Disclaimer: This drug has not been found by FDA to be safe and effective, and this labeling has not been approved by FDA. For further information about unapproved drugs, click here.

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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

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

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

Revised: 7/2023
Document Id: 2b68960c-3c4a-413f-8fa1-8275cfa8d8c4
Set id: 72e889cb-6bd9-43c7-93a3-22038879d36b
Version: 12
Effective Time: 20230706
 
Straight Arrow Products, Inc.