Otc - Active Ingredient
Salicylic Acid 40%
Okkazhie Wart Remover Liquid
FDA Label NDC 87204-201
Full FDA labeling including Indications, Dosage, Usage, and Precautions
Structured Product Label
The following Structured Product Label (SPL) was submitted to the FDA by Guangzhou Huixue Biotechnology Co., Ltd. for the product Okkazhie Wart Remover (NDC 87204-201). 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, inactive ingredient, otc - purpose, indications & usage, warnings, otc - keep out of reach of children, otc - when using, otc - do not use, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Inactive Ingredient
Alcohol Denat., Ethyl Acetate,Pyroxylin, Castor Oil
Otc - Purpose
TARGETS THE WART PRFCISION APPLICATDR FLIMINATE SKIN WARTAND
Indications & Usage
TARGETS THE WART PRFCISION APPLICATDR FLIMINATE SKIN WARTAND，Clean the affected area, apply small amount Apply a small amount Allow to dry Repeat daily as needed
Warnings
If pregnant or nursing, consult a doctor before use
Otc - Keep Out Of Reach Of Children
Store at room temperature. Avoid direct sunlight.
Otc - When Using
1 Clean the affected area 2 Apply a small amount 3 Allow to dry 4 Repeat daily as needed
Otc - Do Not Use
If pregnant or nursing, consult a doctor before use
Otc - Stop Use
Stop use and ask a doctor if irritation occurs or if there is no improvement within 4 weeks.
Dosage & Administration
1 Clean the affected area 2 Apply a small amount 3 Allow to dry 4 Repeat daily as needed
Package Label.Principal Display Panel
Okkazhie WART REMOVER
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