DR. SCHOLLS CLEAR AWAY WART REMOVER PLANTAR- salicylic acid disc

Dr. Scholls by

Drug Labeling and Warnings

Dr. Scholls by is a Otc medication manufactured, distributed, or labeled by Bayer HealthCare LLC.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SPL UNCLASSIFIED SECTION

Drug Facts

Active ingredient

Salicylic acid 40%

Purpose

Wart remover

Uses

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

Warnings

For external use only

Do not use

• if you are a diabetic
• if you have poor blood circulation
• on irritated skin or any area that is infected or reddened
• on moles, birthmarks, warts with hair growing from them, genital warts, or warts on the face or mucous membranes

Stop use and ask a doctor if discomfort lasts

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
• if necessary, cut medicated disc to fit wart
• apply medicated disc directly over wart
• self-adhesive cushioning pads may be used to conceal medicated disc and wart
• repeat procedure every 48 hours as needed (until wart is removed) for up to 12 weeks

Other information

• store between 20° to 25°C (68° to 77°F)
• protect from excessive heat (temperatures above 40°C (104°F))

Inactive ingredients

antioxidant (CAS 991-84-4), iron oxides, mineral oil, petroleum hydrocarbon resin, silicon dioxide, synthetic polyisoprene rubber, talc

Questions?

866-360-3226

PRINCIPAL DISPLAY PANEL - 24 Medicated Disc/24 Cushioning Pads Carton

Dr. Scholl's®

CLEAR

away ®

Wart Remover

Salicylic Acid

Plantar

FOR FEET

• Clinically proven removal
• Relieves pain with
  
  cushioning pad

for Plantar Warts

24 Medicated Disc, 24 Cushioning Pads

INGREDIENTS AND APPEARANCE

DR. SCHOLLS  CLEAR AWAY WART REMOVER PLANTAR
salicylic acid disc

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-0631
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	4 mg

Inactive Ingredients
Ingredient Name	Strength
MINERAL OIL (UNII: T5L8T28FGP)
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)
TALC (UNII: 7SEV7J4R1U)

Product Characteristics
Color	brown	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-0631-1	24 in 1 CARTON; Type 0: Not a Combination Product	08/14/1990	11/30/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	08/14/1990	11/30/2021

Labeler - Bayer HealthCare LLC. (112117283)