Otc - Active Ingredient
ARNICA MONTANA FLOWER
SAFFLOWER
Eelhoe Wart Remover Ointment
FDA Label NDC 85064-005
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shantou Eelhoe Daily Chemical Technology Co., Ltd. for the product Eelhoe Wart Remover (NDC 85064-005). 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, otc - when using, otc - do not use, otc - stop use, otc - keep out of reach of children, warnings, storage and handling, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Natural Herbal Ingredients
Skin Tag & Common Warts Treatment
Otc - When Using
1.Cleanse and dry the affected area.
2.Squeeze wart remover cream.
3.Apply the cream to the surrounding skin cream.
4.Apply it 2 times daily.
Otc - Do Not Use
Discontinue use if signs of irritation or rash occur.
Otc - Stop Use
Discontinue use if signs of irritation or rash occur.
Otc - Keep Out Of Reach Of Children
Please keep out of reach of children. Do not swallow.
Warnings
Please keep out of reach of children. Do not swallow.Please clean your hands before use to ensure the best results from the product. Discontinue use if signs of irritation or rash occur. Store in a cool and dry place.
Storage And Handling
Store in a cool and dry place.
Inactive Ingredient
AQUA、GLYCERIN、MINERAL OIL、GLYCERYL STEARATE、CARBOMER、TRIETHANOLAMINE
Package Label.Principal Display Panel
Label (1)
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