Otc - Active Ingredient
APIS MELLIFERA VENOM、HONEY、ARTEMISIA VULGARIS ROOT
Ximonth Wart Remover Ointment
FDA Label NDC 84989-004
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Shantou Ximonth Biotechnology Co., Ltd. for the product Ximonth Wart Remover (NDC 84989-004). 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, otc - stop use, otc - do not use, otc - when using, otc - keep out of reach of children, inactive ingredient, warnings, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Removes warts and skin tags; Anti-inflammatory and antibacterial; Soothes skin discomfort; Promotes skin cell renewal; Speeds up skin recovery; Maintains skin health
Otc - Stop Use
Discontinue use if signs of irritation or rash occur.
Otc - Do Not Use
Discontinue use if signs of irritation or rash occur.
Otc - When Using
Clean and dry the skin, apply appropriate amount of this product evenly on the affected skin of warts and skin tags, and gently massage until absorbed.
Otc - Keep Out Of Reach Of Children
Please keep out of reach of children. Do not swallow.
Inactive Ingredient
WATER、GLYCERIN、MINERAL OIL、GLYCERYL MONOSTEARATE、CARBOMER HOMOPOLYMER TYPE A、TROLAMINE、ALLANTOIN
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.
Package Label.Principal Display Panel
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Label (Xi B06 0041 01(1))
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