APUREE PRO Nailtific Maximum Strength Antifungal Patches
openFDA label record#
This page contains supplementary openFDA label data. For the canonical label presentation, use the corresponding DailyMed Structured Product Label.
Verified complete openFDA source JSON
- Brand name
- APUREE PRO Nailtific Maximum Strength Antifungal Patches
- Generic name
- APUREE PRO NAILTIFIC MAXIMUM STRENGTH ANTIFUNGAL PATCHES
- Manufacturer
- Guangzhou Meixi Biotechnology Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 5218bd5d-53b4-107f-e063-6394a90ae769
- SPL ID
- 5218bd5d-53b5-107f-e063-6394a90ae769
- Version
- 1
- Effective date
- 2026-05-18
- Source export date
- 2026-10-30
- Source partition
- 3
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0003-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/e1583c3c823c7746dc6fefae78ac97d01bb558f7b0936fc3b7d2e673d3319207/drug-label-0003-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 18:36:49
| Harmonized routes |
|---|
| TOPICAL |
Harmonized identifier links#
Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.
| Type | Scope | Identifier | Source field |
|---|---|---|---|
| application number | M005 | openfda.application_number | |
| brand name | APUREE PRO Nailtific Maximum Strength Antifungal Patches | openfda.brand_name | |
| generic name | APUREE PRO NAILTIFIC MAXIMUM STRENGTH ANTIFUNGAL PATCHES | openfda.generic_name | |
| manufacturer name | Guangzhou Meixi Biotechnology Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 84167-335-01 | openfda.package_ndc |
| ndc | product | 84167-335 | openfda.product_ndc |
| ndc11 | package | 84167033501 | derived:openfda.package_ndc |
| rxcui | 2677690 | openfda.rxcui | |
| spl id | 5218bd5d-53b5-107f-e063-6394a90ae769 | id | |
| spl set id | 5218bd5d-53b4-107f-e063-6394a90ae769 | set_id | |
| unii | 06KB629TKV | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.