DR. SCHOLLS CLEAR AWAY WART REMOVER ONE STEP- salicylic acid disc

Dr. Scholls by

Drug Labeling and Warnings

Dr. Scholls by is a Otc medication manufactured, distributed, or labeled by Bayer Health Care 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 common warts, easily recognized by the rough cauliflower-like appearance of the surface

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
• apply medicated strip, positioning medicated disc directly over wart
• secure adhesive strips firmly to skin
• 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 - 14 Medicated Strips Carton

MAXIMUM



STRENGTH

Dr. Scholl's ®

CLEAR



Away ®



Wart Remover



Salicylic Acid

ONE STEP



Clear Strips

• Clinically proven removal
• Helps prevent the spread
  
  
  
  of the wart virus
• Easy, one step
  
  
  
  application

NET 14 MEDICATED STRIPS

INGREDIENTS AND APPEARANCE

DR. SCHOLLS  CLEAR AWAY WART REMOVER ONE STEP
salicylic acid disc

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-7226
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: 11523-7226-1	14 in 1 CARTON; Type 0: Not a Combination Product	04/12/2005	02/28/2021

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC monograph final	part358B	08/14/1990	02/28/2021

Labeler - Bayer Health Care LLC (112117283)