Premier Solutions Callus Removers

Salicylic acid by

Drug Labeling and Warnings

Salicylic acid by is a Otc medication manufactured, distributed, or labeled by Premier Brands of America Inc.. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

SALICYLIC ACID- callus removers patch 
Premier Brands of America Inc.

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Premier Solutions Callus Removers

​Active ingredient

Salicylic acid 40%

Purpose

Callus remover

Use

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

Warnings

For external use only.

Do not use

  • if you are a diabetic
  • have poor blood circulation
  • on irritated skin, on any area that is infected or reddened

If discomfort persists

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
  • if necessary, cut medicated patch to fit callus
  • carefully adhere medicated patch directly over callus
  • cover medicated patch with pad
  • after 48 hours, remove medicated patch
  • 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

store between 15°C to 30°C (59°F to 86°F)

Inactive ingredients

acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol

Questions?

call 1-866-964-0939

Principal Display Panel

Premier

CALLUS REMOVERS

Salicylic Acid

Effective callus removal treatment

Protects against pressure & friction

MEDICATED

6 PADS/4 MEDICATED PATCHES

image 1

SALICYLIC ACID 
callus removers patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC: 56104-244
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (UNII: O414PZ4LPZ) (SALICYLIC ACID - UNII:O414PZ4LPZ) SALICYLIC ACID40 mg  in 4 
Inactive Ingredients
Ingredient NameStrength
POLYVINYL ALCOHOL (UNII: 532B59J990)  
VINYL ACETATE (UNII: L9MK238N77)  
HIGH DENSITY POLYETHYLENE (UNII: UG00KM4WR7)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC: 56104-244-014 in 1 PACKAGE; Type 0: Not a Combination Product06/16/202212/31/2024
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM03006/16/202212/31/2024
Labeler - Premier Brands of America Inc. (063849780)

Revised: 8/2025
Document Id: 3bba69a2-c7c8-e420-e063-6294a90a8741
Set id: e192e81a-b7f9-3461-e053-2995a90a7e2c
Version: 5
Effective Time: 20250806