warnings
WARNINGS: KEEP OUT OF REACH OF CHILDREN. This product is flammable. Keep away from fire or flame. Keep bottle tightly closed when not in use.
XALIX
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
- XALIX
- Generic name
- SALICYLIC ACID
- Manufacturer
- Cintex Services, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 41369b38-7f15-b597-e063-6394a90a614b
- SPL ID
- 41369805-8394-c804-e063-6394a90a0440
- Version
- 1
- Effective date
- 2025-10-15
- Source export date
- 2026-11-06
- Source partition
- 2
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0002-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-11-06/4dafeb36642dffb72e2138939a956de402f722ea8c14c08cd87068efd3669f01/drug-label-0002-of-0014.json.zip
- Source manifest SHA-256
- 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
- Import run
- 20261108T063105Z
- Imported at
- 2026-11-08 06:47:33
| 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 |
|---|---|---|---|
| brand name | XALIX | openfda.brand_name | |
| generic name | SALICYLIC ACID | openfda.generic_name | |
| manufacturer name | Cintex Services, LLC | openfda.manufacturer_name | |
| ndc | package | 24470-947-10 | openfda.package_ndc |
| ndc | product | 24470-947 | openfda.product_ndc |
| ndc11 | package | 24470094710 | derived:openfda.package_ndc |
| rxcui | 1986360 | openfda.rxcui | |
| rxcui | 1986365 | openfda.rxcui | |
| spl id | 41369805-8394-c804-e063-6394a90a0440 | id | |
| spl set id | 41369b38-7f15-b597-e063-6394a90a614b | set_id | |
| unii | O414PZ4LPZ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
Adverse reactions cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
adverse reactions
ADVERSE REACTIONS: Localized irritation may occur if this product is applied to normal skin surrounding the wart; however irritation may normally be controlled by temporarily discontinuing use and by applying the medication only to the wart site when treatment is resumed. To report a serious adverse event, call 1-855-899-4237.
Reported adverse events (FAERS/openFDA)#
Adverse event summaries are temporarily unavailable. Other product information remains available.