warnings
Warnings For external use only.
Subleef SKIN WART CORN 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
- Subleef SKIN WART CORN REMOVER
- Generic name
- WART CORN REMOVER
- Manufacturer
- Putian Licheng District Zhijiancheng Trading Co., Ltd.
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 54aeb166-d703-1d23-e063-6394a90a19a4
- SPL ID
- 54aeb166-d704-1d23-e063-6394a90a19a4
- Version
- 1
- Effective date
- 2026-06-20
- Source export date
- 2026-10-30
- Source partition
- 8
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-30/023bc8d8aae5addb7530087bbbdb169b3ccbf36764f15b8ca67db07e1e5aea8b/drug-label-0008-of-0014.json.zip
- Source manifest SHA-256
- b11f1f6b476c7417db937215bf14307ef1a0b69465b42b411ad52f42ae36ead3
- Import run
- 20261102T182004Z
- Imported at
- 2026-11-02 19:09:49
| 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 | M030 | openfda.application_number | |
| brand name | Subleef SKIN WART CORN REMOVER | openfda.brand_name | |
| generic name | WART CORN REMOVER | openfda.generic_name | |
| manufacturer name | Putian Licheng District Zhijiancheng Trading Co., Ltd. | openfda.manufacturer_name | |
| ndc | package | 87152-005-01 | openfda.package_ndc |
| ndc | product | 87152-005 | openfda.product_ndc |
| ndc11 | package | 87152000501 | derived:openfda.package_ndc |
| rxcui | 312881 | openfda.rxcui | |
| spl id | 54aeb166-d704-1d23-e063-6394a90a19a4 | id | |
| spl set id | 54aeb166-d703-1d23-e063-6394a90a19a4 | 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.