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Visco-Gel Medicated Round Callus Removers

Dosage form: disc
Ingredients: SALICYLIC ACID 17.67mg
Labeler: PEDIFIX, INC.
NDC Code: 68927-0819

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.

Visco-GEL® Medicated Round 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-PEDIFIX (733-4349)

PRINCIPAL DISPLAY PANEL - 4 Disk Blister Pack

PediFix®
The Podiatrist's Choice
Since 1885

NEW!

Visco-GEL®
Medicated Round
Callus Removers
With Salicylic Acid

Instant Pain Relief!

  • Safely Removes Calluses
  • Adhesive Gel Cushions
    & Protects

Relief
Spot

Maximum
Strength

Washable & Reusable
Effective for Weeks

4 Medicated Disks
4 Cushions

VISCO-GEL MEDICATED ROUND CALLUS REMOVERS 
salicylic acid disc
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:68927-0819
Route of AdministrationTOPICALDEA Schedule    
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
SALICYLIC ACID (SALICYLIC ACID) SALICYLIC ACID17.67 mg
Inactive Ingredients
Ingredient NameStrength
POLYVINYL ALCOHOL 
HIGH DENSITY POLYETHYLENE 
VINYL ACETATE 
Packaging
#Item CodePackage Description
1NDC:68927-0819-14 DISC in 1 BLISTER PACK
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC MONOGRAPH FINALpart358F06/01/2013
Labeler - PEDIFIX, INC. (122271935)
Establishment
NameAddressID/FEIOperations
PEDIFIX, INC.122271935LABEL(68927-0819), PACK(68927-0819)
Establishment
NameAddressID/FEIOperations
AKRON186569323MANUFACTURE(68927-0819)

 
PEDIFIX, INC.

Medically reviewed on Aug 27, 2018

Further information

Always consult your healthcare provider to ensure the information displayed on this page applies to your personal circumstances.

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