warnings
Warnings（警告） For external use only. Keep away from fire and flame.
Alveora CORN WART REMOVER
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
- Alveora CORN WART REMOVER
- Generic name
- ALVEORA CORN WART REMOVER
- Manufacturer
- Jiangxi Yudexi Pharmaceutical Co., LTD
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 49a7e214-74b8-0cbd-e063-6394a90a2e9c
- SPL ID
- 49a7e214-74b9-0cbd-e063-6394a90a2e9c
- Version
- 1
- Effective date
- 2026-01-30
- Source export date
- 2026-11-06
- Source partition
- 4
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 07:03:15
| 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 | M028 | openfda.application_number | |
| brand name | Alveora CORN WART REMOVER | openfda.brand_name | |
| generic name | ALVEORA CORN WART REMOVER | openfda.generic_name | |
| manufacturer name | Jiangxi Yudexi Pharmaceutical Co., LTD | openfda.manufacturer_name | |
| ndc | package | 85248-034-01 | openfda.package_ndc |
| ndc | product | 85248-034 | openfda.product_ndc |
| ndc11 | package | 85248003401 | derived:openfda.package_ndc |
| rxcui | 312881 | openfda.rxcui | |
| spl id | 49a7e214-74b9-0cbd-e063-6394a90a2e9c | id | |
| spl set id | 49a7e214-74b8-0cbd-e063-6394a90a2e9c | set_id | |
| unii | O414PZ4LPZ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.