VERRUSTAT WART REMOVER- salicylic acid liquid

VerruStat Wart Remover by

Drug Labeling and Warnings

VerruStat Wart Remover by is a Otc medication manufactured, distributed, or labeled by Clinical Therapeutic Solutions. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

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

VerruStat Liquid Wart Remover 15ml (

44577-020-15)

INGREDIENTS AND APPEARANCE

VERRUSTAT WART REMOVER 
salicylic acid liquid

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44577-020
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	170 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
BUTYL ACETATE (UNII: 464P5N1905)
ETHYL ACETATE (UNII: 76845O8NMZ)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
PYROXYLIN (UNII: KYR8BR2X6O)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)
ALCOHOL (UNII: 3K9958V90M)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44577-020-15	1 in 1 BOX	02/06/2017
1		15 mL in 1 BOTTLE, WITH APPLICATOR; Type 0: Not a Combination Product

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	10/16/2013

Labeler - Clinical Therapeutic Solutions (078402750)