SALICYLIC ACID- medicated callus removers extra thick patch 
Target Corporation

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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Target Extra Thick Callus Removers

Active ingredient

Salicylic acid 40%

Purpose

Callus remover

Use

Warnings

For external use only.

Do not use

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

Stop use and ask a doctor

if discomfort persists

Keep out of reach of children.

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

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

medicated

callus removers

salicylic acid 40%

effective callus removal treatment

extra thick pads cushion & help

protect against pressure & friction

4 PADS/ 4 MEDICATED PATCHES

up&up_Extra Thick Callus Removers_52-072TG.jpg

SALICYLIC ACID 
medicated callus removers extra thick patch
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:11673-631
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:11673-631-044 in 1 PACKAGE; Type 0: Not a Combination Product12/01/2017
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC monograph finalpart358F12/01/2017
Labeler - Target Corporation (006961700)

Revised: 7/2021
Document Id: c7b63cd2-58dd-0b31-e053-2a95a90a7ac9
Set id: 6e2509ab-ec8f-4e2d-b1b5-0b547a11d319
Version: 4
Effective Time: 20210722
 
Target Corporation