Walgreens Medicated Corn Removers Patch
FDA Label NDC 0363-2025
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Walgreen Co. for the product Walgreens Medicated Corn Removers (NDC 0363-2025). 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 drug facts, active ingredient (in each dosage unit), purposes, uses, warnings, otc - keep out of reach of children, directions, other information, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Active Ingredient (In Each Dosage Unit)
Salicylic acid 40% in a plaster vehicle
Purposes
Corn and calluses removal
Uses
• For the removal of corns and calluses
• Relieves pain by removing corns and calluses
• Adhesive bandage holds the medicated pad in position
Warnings
For external use only
Do not use
• If you are a diabetic
• If you have poor blood circulation
• On irritated skin or any area that is infected or reddened
Stop use and ask a doctor if
Discomfort lasts
Otc - Keep Out Of Reach Of Children
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 after 48 hours, remove medicated bandage
• 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 0° to 40°C (32° to 104°F)
Inactive Ingredients
Pressure sensitive adhesive fabric
Questions?
1-800-723-2465
Packaging
Walgreens-6045 (0363202509)
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