warnings
The liquid can get easily volatilized & crystalllzed, tighten the cap after use. Avoid long-term contact with alr while using. For external use only,don't contact with eyes or swallow, Children should use it under the supervision of adults.
WART REMOVER (salicylic acid) liquid
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
- WART REMOVER (salicylic acid) liquid
- Generic name
- SALICYLIC ACID
- Manufacturer
- Shenzhen Finona Information Technology Co., Ltd
- Product type
- HUMAN OTC DRUG
- SPL set ID
- 3871fbd4-7eb6-0cdc-e063-6394a90abd08
- SPL ID
- 452ce5b0-4960-47f1-e063-6294a90aaab0
- Version
- 4
- Effective date
- 2025-12-04
- Source export date
- 2026-11-06
- Source partition
- 13
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/245ea1c0d730b312e4410f082201cbe2cb4d1936fa2918316b6ea631293cbeba/drug-label-0013-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 08:09:59
| 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 | WART REMOVER (salicylic acid) liquid | openfda.brand_name | |
| generic name | SALICYLIC ACID | openfda.generic_name | |
| manufacturer name | Shenzhen Finona Information Technology Co., Ltd | openfda.manufacturer_name | |
| ndc | package | 85839-003-01 | openfda.package_ndc |
| ndc | product | 85839-003 | openfda.product_ndc |
| ndc11 | package | 85839000301 | derived:openfda.package_ndc |
| rxcui | 198845 | openfda.rxcui | |
| spl id | 452ce5b0-4960-47f1-e063-6294a90aaab0 | id | |
| spl set id | 3871fbd4-7eb6-0cdc-e063-6394a90abd08 | 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.