FDA Label for Verrustat Wart Remover

View Indications, Usage & Precautions

Verrustat Wart Remover Product Label

The following document was submitted to the FDA by the labeler of this product Clinical Therapeutic Solutions. The document includes published materials associated whith this product with the essential scientific information about this product as well as other prescribing information. Product labels may durg indications and usage, generic names, contraindications, active ingredients, strength dosage, routes of administration, appearance, warnings, inactive ingredients, etc.

Active Ingredient



Salicylic Acid 17%


Purpose



wart treatment


Uses:



  • For the removal of common and plantar warts. The common wart has a rough 'cauliflower-like' appearance. The plantar wart exists only on the bottom of the foot  and interrupts the footprint pattern.

Warnings



For external use only. Do not use this product on irritated skin, on any area that is infected or reddened, if you are a diabetic, or if you have poor blood circulation. If discomfort persists, see your doctor. Do not use on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes. Flammable. Keep away from fire or flame. Cap bottle tightly and store at room temperature away from heat. If product gets into the eye, flush with water for 15 minutes. Avoid inhaling vapors.


Directions



  • wash or soak the affected area and dry thoroughly
  • apply wart remover liquid, with enclosed applicator
  • reapply subsequent applications over existing application
  • repeat the procedure once or twice daily, until wart is completely removed, for up to 12 weeks

Other Information



  • Store between 20 degrees to 30 degrees C (68 degrees to 86 degrees F)



Other Ingredients



Butyl Acetate, Ethyl Acetate, Isopropyl Alcohol, Methylsulfonylmethane (MSM), Nitrocellulose, Retinyl Palmitate, SD-Alcohol 40B


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