Active Ingredient
Salicylic acid 40%
Mymulike Corn Removal Pads Patch
FDA Label NDC 83781-003
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Zhengzhou Miaoqi Pharmaceutical Technology Co., Ltd for the product Mymulike Corn Removal Pads (NDC 83781-003). 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, stop use, ask doctor, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Purpose
Corn and callus remover
Use
for the removal of corns from foot and hand.
Warnings
for external use only
Do Not Use
on irritated skin or any area that is infected or reddened.
When Using
if product gets in eyes,flush with water for 15 minutes.
Ask a doctor before use if you have
■diabetes
■poor blood circulation
■under 14 years old
■pregnant and lactating women
Stop Use
discomfort persists.
Ask Doctor
discomfort persists.
Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Directions
■Wash affected corn and dry thoroughly.
■Please cut the medicated patch as a suitable size to cover your corn.
■Place frmly the medicated round part over the center of corn. Adhesive next to skin.
■Repeart the treatment as need until corn is removed. (The result may vary from person.)
■May soak corn in warm water for 5 minutes to assist in the removal.
Other Information
store between 20°to 25℃ (68°to 77℉)
Inactive Ingredients
hard paraffin, lanolin, phenol
Questions
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