DR. SCHOLLS CALLUS REMOVERS- salicylic acid disc 
Bayer HealthCare LLC.

Disclaimer: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

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Dr. Scholl's ® Callus REMOVERS Salicylic Acid

Drug Facts

Active Ingredients

Salicylic acid 40%

Purpose

Callus Remover

Warnings

For external use only

Do not use

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

Uses

Uses

  • for the removal of calluses
  • relieves pain by removing calluses

Ask a doctor before use if you have

Ask a doctor before use if you have if discomfort lasts

Keep out of reach of children

Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away.

Directions

Directions

▪ wash affected area and dry thoroughly

▪ if necessary, cut medicated disc to fit callus

▪ apply medicated disc with sticky side adhering to skin

▪ cover medicated disc with enclosed cushion

▪ after 48 hours, remove medicated disc

▪ repeat procedure every 48 hours as needed for up to 14 days (until callus is removed)

▪ may soak callus in warm water for 5 minutes to assist in removal

Other information

Other information

▪ Store between 20° to 25°C (68° to 77°F).

▪ Protect from excessive heat (temperatures above 40°C (104°F)).

Inactive Ingredients

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

Questions or Comments

Questions or Comments? 1- 866-360-3226

Dr. Scholls Callus Remover Package

DR. SCHOLLS  CALLUS REMOVERS
salicylic acid disc
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11523-0465
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID0.4 g
Inactive Ingredients
Ingredient NameStrength
MINERAL OIL (UNII: T5L8T28FGP)  
SILICON DIOXIDE (UNII: ETJ7Z6XBU4)  
TALC (UNII: 7SEV7J4R1U)  
Product Characteristics
Colorbrown (opaque solid) Score    
ShapeSize
FlavorImprint Code
Contains    
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:11523-0465-11 in 1 CARTON08/14/199009/30/2018
14 in 1 CELLO PACK; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F08/14/199009/30/2018
Labeler - Bayer HealthCare LLC. (112117283)

Revised: 8/2017
 
Bayer HealthCare LLC.