Otc - Active Ingredient
Salicylic acid 40%
Corn Remover Pads Patch
FDA Label NDC 85839-004
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 Finona Information Technology Co., Ltd for the product Corn Remover Pads (NDC 85839-004). 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 otc - active ingredient, otc - purpose, indications & usage, warnings, otc - do not use, otc - when using, otc - keep out of reach of children, dosage & administration, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Corn Remover
Indications & Usage
for the removal of corns relieves pain by removing corns
Warnings
For external use only.
Otc - Do Not Use
If your have poor blood cireulation
lf you are dlabetic, pregnant or breastfeeding
On irritated skin or on any area that is infected or reddened
Otc - When Using
If discomfort persists see your doctor or podiatrist
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Dosage & Administration
Wash affected area and dry thoroughily
Place firmly the medicated round part over the center of corn, adhesive next to skin.(if necessary, cut the medicated patch to fit cor.)
Repeat the treatment dally as needed forup to 14 days (untll corn is removed)
May soak corn in warm water for 5 minutes to assist in the removal
Inactive Ingredient
mugwort
safflower
lanolin
phenol
vaseline
hot glue
Package Label.Principal Display Panel
Label4 (Label4)
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