Active Ingredient
Salicylic acid 40%
Salicylic Acid Patch
FDA Label NDC 36800-373
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Topco Associates Llc for the product Salicylic Acid (NDC 36800-373). 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, use, warnings, do not use, stop use and ask a 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
Use
- for the removal of calluses
- relieves pain by removing calluses
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
- wash affected area and dry area thoroughly
- if necessary, cut medicated patch to fit callus
- apply adhesive side down of medicated patch onto 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 corn is removed)
- may soak corn 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
topCare
Medicated
Extra Thick Callus Removers
with SALICYLIC ACID
Protects against pressure & pain
Callus removal treatment
4 PADS
4 MEDICATED PATCHES
* Please review the disclaimer below.
