APUREE Nailtific Maximum Strength Antifungal Patches PRO
APUREE Nailtific Maximum Strength Antifungal Patches PRO is an FDA drug label for the active ingredient APUREE NAILTIFIC MAXIMUM STRENGTH ANTIFUNGAL PATCHES PRO manufactured by Guangzhou Meixi Biotechnology Co., Ltd administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260511.
- Generic name
- APUREE NAILTIFIC MAXIMUM STRENGTH ANTIFUNGAL PATCHES PRO
- Manufacturer
- Guangzhou Meixi Biotechnology Co., Ltd
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 84167-416
- Application
- M005
- Label effective
- 20260511
About this product
APUREE Nailtific Maximum Strength Antifungal Patches PRO is an FDA-registered drug product whose active ingredient is APUREE NAILTIFIC MAXIMUM STRENGTH ANTIFUNGAL PATCHES PRO. It is labelled by Guangzhou Meixi Biotechnology Co., Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 84167-416, application M005, label effective 20260511. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.
Active ingredients
Indications & Usage
Antifungal
Dosage & Administration
8 Hour
Warnings
keep out of children
Frequently asked questions
What is APUREE Nailtific Maximum Strength Antifungal Patches PRO used for?
Antifungal
Who makes APUREE Nailtific Maximum Strength Antifungal Patches PRO?
Guangzhou Meixi Biotechnology Co., Ltd is the labeler of record for APUREE Nailtific Maximum Strength Antifungal Patches PRO.
What form does APUREE Nailtific Maximum Strength Antifungal Patches PRO come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is APUREE Nailtific Maximum Strength Antifungal Patches PRO prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.
Has APUREE Nailtific Maximum Strength Antifungal Patches PRO been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.
Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.