Active Ingredient
Salicylic Acid 40%
Supreh Corn Remover Pads Patch
FDA Label NDC 83818-032
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shenzhen Xinxin Yunhai Technology Co., Ltd. for the product Supreh Corn Remover Pads (NDC 83818-032). 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, when using this product, stop use and ask a doctor if, keep out of reach of children, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Corn Remover
Use
for the removal of corns
relieves pain by removing corns
Warnings
For external use only.
Do Not Use
on irritated or infected skin
if you have diabetes
if you have poor blood circulation
When Using This Product
avoid contact with eyes
do not use on any area of the body except as directed
Stop Use And Ask A Doctor If
irritation occurs
symptoms persist for more than 14 days
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.
apply medicated bandage over the center of corn.
after 24 hours, remove medicated bandage.
repeat procedure every 24 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 at 15–30°C (59–86°F)
protect from excessive heat above 40°C (104°F)
Inactive Ingredients
borneol, camphor, safflower oil, sessile stemona root extract, titanium dioxide
Questions
TEL: +1 858905 0218
[email protected]
Principal Display Panel
1 (Pack)
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