Otc - Active Ingredient
Salicylic acid 17%
Aemerry Wart Corn Callus Remover Liquid
FDA Label NDC 87615-003
10 label sections · Submitted to the FDA by Da Capo Prima Llc · Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Da Capo Prima Llc for the product Aemerry Wart Corn Callus Remover (NDC 87615-003). 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 otc - active ingredient, otc - purpose, dosage & administration, indications & usage, warnings, otc - do not use, otc - ask doctor/pharmacist, otc - 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
Otc - Purpose
Wart Remover
Dosage & Administration
For the removal of common warts, plantar warts, corns, and calluses.
Indications & Usage
- Soak the affected area in warm water for 5 minutes. Dry thoroughly.
- Remove the inner plug from the bottle. Attach the brush applicator securely.
- Apply directly to the wart or corn using the brush.
- Apply twice daily for up to 2 weeks.
- For larger warts or corns, continue use as needed.
Warnings
For external use only.
Otc - Do Not Use
- If you have poor blood circulation.
- If you are diabetic, pregnant, or breastfeeding.
- On irritated skin or any area that is infected or reddened.
Otc - Ask Doctor/Pharmacist
- Discomfort persists or condition worsens.
- If you are allergic to this product.
Otc - Keep Out Of Reach Of Children
If swallowed, get medical help or contact a Poison Control Center right away.
Inactive Ingredient
Water, Glycerin, Borneol, Lonicera, Japonica Flower Extract
Package Label.Principal Display Panel
Package (Package)
package
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