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
- DEA Schedule: None
- Marketing Status: unapproved drug other
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Drug Label Information
Updated July 6, 2023
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- Active Ingredient:
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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:
- General Precautions:
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
PRO-TECT HOT SPOT SKIN MEDICATION
benzalkonium chloride liquidProduct Information Product Type OTC ANIMAL DRUG Item Code (Source) NDC:62001-0317 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) (BENZALKONIUM - UNII:7N6JUD5X6Y) BENZALKONIUM CHLORIDE .001 g in 1 g Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:62001-0317-1 118 g in 1 BOTTLE, PLASTIC Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date unapproved drug other 09/25/2003 Labeler - Straight Arrow Products, Inc. (061580593) Registrant - Straight Arrow Products, Inc. (061580593) Establishment Name Address ID/FEI Business Operations Straight Arrow Products, Inc. 052165154 manufacture, pack Establishment Name Address ID/FEI Business Operations Lonza Biologics, Inc. 093149750 api manufacture