Otc - Active Ingredient
Tolnaftate
Apuree Nailtific Extra-max Strength Nighttime Antifungal Liquid
FDA Label NDC 84167-479
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 Nighttime Antifungal (NDC 84167-479). 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, dosage & administration, otc - keep out of reach of children, indications & usage, otc - purpose, 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
Dosage & Administration
Apply directly to the affected area
Otc - Keep Out Of Reach Of Children
keep out of reach of child
Indications & Usage
Antibacterial and anti-itch
Otc - Purpose
15-Day & 15-Night Supply
Inactive Ingredient
Simmondsia Chinensis Seed Oil,Caprylic/Capric Triglyceride,Pentaerythrityl Tetra-Di-T-Butyl Hydroxyhydrocinnamate,Melaleuca Alternifolia Leaf Oil,Cinnamomum Cassia Oil,Origanum Vulgare Oil,Calophyllum Inophyllum Seed Oil,Eugenia Caryophyllus Bud Oil,Eucalyptus Globulus Leaf Oil,Lavandula Angustifolia Oil
Package Label.Principal Display Panel
22 (22)
* Please review the disclaimer below.
