Otc - Active Ingredient
Salicylic Acid 17% w/w
PurposeWart remover
Olnuitexl Wart Remover Liquid
FDA Label NDC 85593-124
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 Chuanma International Trading Co.,ltd. for the product Olnuitexl Wart Remover (NDC 85593-124). 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 - keep out of reach of children, warnings, dosage & administration, indications & usage, inactive ingredient, package label.principal display panel, and other regulatory disclosures. Use the navigation below to review specific sections of the FDA submission.
Label Section Quick Index
Otc - Purpose
Uses
For the removal of warts, including plantar warts, flatwarts, common warts, corns, and calluses.
Otc - Keep Out Of Reach Of Children
Keep out of reach of children.
Warnings
Warnings
For external use only.
Flammable: keep away from fire and flame.
Dosage & Administration
Take an appropriate amount and apply to the corresponding area.
Indications & Usage
On broken skin or the area around the eyes.On irritated skin or on any area that is infected orreddened.
Inactive Ingredient
Inactive Ingredients
Alcohol, Propylene Glycol, Water, Lactic Acid,Pentylene Glycol
Package Label.Principal Display Panel
85593-124-01 (85593 124 01)
* Please review the disclaimer below.
