WALGREENS MEDICATED CALLUS REMOVERS- salicylic acid disc 
WALGREENS Co.

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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Walgreens Medicated Gel Callus Removers

Drug Facts

Active Ingredient

Salicylic acid 40%

Purpose

Callus remover

Uses

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

Warnings

For external use only   Use only as directed

Do Not Use

  • if you are diabetic
  • on irritated, broken or infected skin
  • if you have poor blood circulation

If discomfort persists, see your doctor or podiatrist.

KEEP OUT OF REACH OF CHILDREN. If swallowed, get medical help or contact a Poison Control center immediately.

Directions

  • Wash affected area. Soak in warm water for 5 minutes if desired.
    Dry thoroughly
  • Apply medicated disk directly over callus
  • Cover medicated disk with gel pad
  • After 48 hours, remove medicated disk
  • Repeat procedure every 48 hours as needed (until callus is removed) for up to 14 days

Other Information

Store between 59° and 86°F (15° and 30°C)

Inactive Ingredients

Polyvinyl Alcohol, Acrylic Copolymer

Questions or Comments?

CALL: 1-800-925-4733

DISTRIBUTED BY: WALGREEN CO.
200 WILMOT RD., DEERFIELD, IL 60015

PRINCIPAL DISPLAY PANEL - 4 Disk Blister Pack

Well at
Walgreens

WALGREENS PHARMACIST RECOMMENDED

NEW

MEDICATED

Gel Callus
Removers

Salicylic Acid 40%

  • Callus removal treatment
  • Cushions against pressure & pain
  • Self-sticking, washable & reusable
  • Effective for weeks

4
MEDICATED
DISKS | 4 CUSHIONS

PRINCIPAL DISPLAY PANEL - 4 Disk Blister Pack
WALGREENS MEDICATED CALLUS REMOVERS 
salicylic acid disc
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:0363-0819
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID17.67 mg  in 44.18 mg
Inactive Ingredients
Ingredient NameStrength
POLYVINYL ALCOHOL (UNII: 532B59J990)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
VINYL ACETATE (UNII: L9MK238N77)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:0363-0819-011 in 1 CONTAINER06/01/2013
14 in 1 CELLO PACK
144.18 mg in 1 PATCH; Type 0: Not a Combination Product
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F06/01/2013
Labeler - WALGREENS Co. (008965063)
Registrant - PEDIFIX, INC. (122271935)
Establishment
NameAddressID/FEIBusiness Operations
PEDIFIX122271935pack(0363-0819) , label(0363-0819)
Establishment
NameAddressID/FEIBusiness Operations
AKRON186569323manufacture(0363-0819)

Revised: 3/2023
 
WALGREENS Co.