DR. SCHOLLS CORN/CALLUS REMOVER- salicylic acid solution

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 17%

Purpose

Corn and callus remover

Uses

• for removal of corns and calluses
• relieves pain by removing corns and calluses

Warnings

For external use only

Flammable Keep away from fire or flame

Do not use

• if you have diabetes
• if you have poor blood circulation
• on irritated skin or any area that is infected or reddened

When using this product

• if product gets in eyes, flush with water for 15 minutes
• do not inhale vapors
• cap bottle tightly and store at room temperature away from heat

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 and dry thoroughly
• apply one drop at a time with applicator to sufficiently cover each corn/callus
• let dry
• repeat procedure once or twice daily as needed for up to 14 days (until corn/callus is removed)
• may soak corn/callus in warm water for 5 minutes to assist in removal
• protective pads may be used to cushion corn/callus during treatment

Other information

• store between 20° to 25°C (68° to 77°F)
• keep tightly closed
• retain card for full labeling

Inactive ingredients

castor oil, ethyl lactate, flexible collodion, polybutene. (Contains alcohol 18% v/v and ether 53%v/v from flexible collodion).

Questions?

866-360-3226

PRINCIPAL DISPLAY PANEL - 9.8 mL Bottle Blister Pack

UPC 26200

Dr Scholl's®

LiquidCorn/Callus

REMOVER

Salicylic

Acid

Removes

Corns/Calluses

Fast

• Corn cushions
  
  provide
  
  immediate
  
  & all-day
  
  pain relief

Net 3 CUSHIONS

1/3 FL OZ (9.8 mL)

INGREDIENTS AND APPEARANCE

DR. SCHOLLS  CORN/CALLUS REMOVER
salicylic acid solution

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 11523-0464
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ)	SALICYLIC ACID	1.7 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
CASTOR OIL (UNII: D5340Y2I9G)
ETHYL LACTATE (UNII: F3P750VW8I)
ALCOHOL (UNII: 3K9958V90M)
ETHER (UNII: 0F5N573A2Y)

Product Characteristics
Color	yellow (clear yellow)	Score
Shape		Size
Flavor		Imprint Code
Contains

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 11523-0464-1	1 in 1 BLISTER PACK	08/14/1990	01/31/2021
1		9.8 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	part358F	08/14/1990	01/31/2021

Labeler - Bayer HealthCare LLC. (112117283)