APUREE Nailtific Extra-Max Strength Nighttime Antifungal
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 Nailtific Extra-Max Strength Nighttime Antifungal
- Generic name
- APUREE NAILTIFIC EXTRA-MAX STRENGTH NIGHTTIME ANTIFUNGAL
- Manufacturer
- Guangzhou Meixi Biotechnology Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 4e3e8895-34b4-de69-e063-6294a90a5532
- SPL ID
- 4e3e8895-34b5-de69-e063-6294a90a5532
- Version
- 1
- Effective date
- 2026-03-30
- Source export date
- 2026-11-06
- Source partition
- 10
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b0d9ca61dc485ebaf55e14a76d7d677668e40ef1e1978cdbcc4d73d58eba0b99/drug-label-0010-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:45:35
| 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 Nailtific Extra-Max Strength Nighttime Antifungal | openfda.brand_name | |
| generic name | APUREE NAILTIFIC EXTRA-MAX STRENGTH NIGHTTIME ANTIFUNGAL | openfda.generic_name | |
| manufacturer name | Guangzhou Meixi Biotechnology Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 84167-479-02 | openfda.package_ndc |
| ndc | product | 84167-479 | openfda.product_ndc |
| ndc11 | package | 84167047902 | derived:openfda.package_ndc |
| rxcui | 313423 | openfda.rxcui | |
| spl id | 4e3e8895-34b5-de69-e063-6294a90a5532 | id | |
| spl set id | 4e3e8895-34b4-de69-e063-6294a90a5532 | set_id | |
| unii | 06KB629TKV | openfda.unii |
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.