VERRUSTAT MEDICATED PLANTAR PADS- salicylic acid patch

VerruStat Medicated Plantar Pads by

Drug Labeling and Warnings

VerruStat Medicated Plantar Pads 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 40%

Purpose

wart remover

Uses:

• For the removal of plantar warts on the bottom of the foot. The plantar wart is recognized by its location only on the bottom of the foot, its tenderness and interruption of the footprint pattern.

Warnings

For external use only.

Do not use

• on irritated skin
• on any area that is infected or reddened
• on moles
• on birthmarks
• on warts with hair growing from them
• on genital warts
• on warts on the face
• on warts on mucous membranes such as inside the mouth, nose, anus, genitals, lips
  

Ask a doctor before use if you have

• diabetes
• poor blood circulation
  

Stop use and ask a doctor if

• discomfort persists.
  

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

• Wash affected area
• May soak wart in warm water for 5 minutes
• Dry area thoroughly
• Remove medicated pad from backing paper
• Apply
• Repeat procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other Information

• Store at room temperature
• Avoid excessive heat (37 degrees C, 99 degrees F)
  

Inactive Ingredients

Lanolin, Paraffin, Petrolatum, Phenol, Retinal Palmitate

VerruStat Medicated Plantar Pads 20 Pads (

44577-040-20)

INGREDIENTS AND APPEARANCE

VERRUSTAT MEDICATED PLANTAR PADS  
salicylic acid patch

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 44577-040
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	0.4 g  in 100 g

Inactive Ingredients
Ingredient Name	Strength
LANOLIN (UNII: 7EV65EAW6H)
PARAFFIN (UNII: I9O0E3H2ZE)
PETROLATUM (UNII: 4T6H12BN9U)
PHENOL (UNII: 339NCG44TV)
VITAMIN A PALMITATE (UNII: 1D1K0N0VVC)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 44577-040-20	20 in 1 BOX	02/05/2017
1		0.5 g in 1 PATCH; Type 2: Prefilled Drug Delivery Device/System (syringe, patch, etc.)

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)