Active Ingredient
Salicylic acid 40%
Medicated Callus Removers
FDA Label NDC 79481-0593
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Meijer Distribution Inc. for the product Medicated Callus Removers (NDC 79481-0593). This document serves as the official prescribing information, containing essential scientific data and clinical materials required for healthcare providers and patients.
This specific version of the label includes detailed information regarding active ingredient, purpose, uses, warnings, do not use, ask your doctor, keep out of reach of children., directions, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Callus remover
Uses
- for removal of calluses
- relieves pain by removing calluses
Warnings
For external use only.
Do Not Use
- if you are diabetic
- if you have poor blood circulation
- on irritated skin,on any area that is infected or reddened
Ask Your Doctor
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° to 86°F)
Inactive Ingredients
acrylic adhesive, acrylic polymer, polyethylene, polyvinyl alcohol
Questions?
call 1-866-964-0939
Principal Display Panel
Kroger
Medicated
callus remover
SALICYLIC ACID 40%
Maximum Strength
- Effective Callus Remover Treatment
- Protects Against Pressure & Friction
6 PADS
4 MEDICATED PATCHES
* Please review the disclaimer below.
