Warnings
keep out of reach of children section
Apuree Nailtific Extra-max Strength Daytime Antigungal Liquid
FDA Label NDC 84167-423
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 Meixi Biotechnology Co., Ltd. for the product Apuree Nailtific Extra-max Strength Daytime Antigungal (NDC 84167-423). 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 warnings, otc - keep out of reach of children, otc - purpose, otc - active ingredient, inactive ingredient, indications & usage, dosage & administration, 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 - Keep Out Of Reach Of Children
keep out of reach of children
Otc - Purpose
Antibacterial and anti-itch
Otc - Active Ingredient
Undecylenic Acid,Tolnaftate
Inactive Ingredient
PEG-8,Alcohol Denat,PEG-40 Hydrogenated Castor Oil,Menthol,Aqua,Origanum Vulgare Oil,Eugenia Caryophyllus Bud Oil,Cinnamomum Cassia Oil,Calophyllum Inophyllum Seed Oil,Melaleuca Alternifolia Leaf Oil,Eucalyptus Globulus Leaf Oil,Salicylic Acid
Indications & Usage
15-Day & 15-Night Supply, 1.5 ml e 0.05 f. oz. each l Total 45 ml l 1.52 f. oz.
Dosage & Administration
Apply directly to the affected area
Package Label.Principal Display Panel
3 (1)
* Please review the disclaimer below.
