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.
SALICYLIC ACID
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
- SALICYLIC ACID
- Generic name
- SALICYLIC ACID
- Manufacturer
- Cintex Services, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 41371177-2e79-f7b0-e063-6294a90a747a
- SPL ID
- 41371183-bf33-3d47-e063-6394a90a094e
- Version
- 1
- Effective date
- 2025-10-15
- Source export date
- 2026-10-27
- Source partition
- 12
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-10-27/977776a6cc37ec1c77259da8a93ae161850a3aa120341096e5a03428b84d016b/drug-label-0012-of-0014.json.zip
- Source manifest SHA-256
- 6be3667a3beefe6c0ead4c723ea963050533a2bc725a8044d58b07d18b258c55
- Import run
- 20261027T193451Z
- Imported at
- 2026-10-27 20:58:34
| 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 | SALICYLIC ACID | openfda.brand_name | |
| generic name | SALICYLIC ACID | openfda.generic_name | |
| manufacturer name | Cintex Services, LLC | openfda.manufacturer_name | |
| ndc | package | 24470-949-10 | openfda.package_ndc |
| ndc | product | 24470-949 | openfda.product_ndc |
| ndc11 | package | 24470094910 | derived:openfda.package_ndc |
| rxcui | 312887 | openfda.rxcui | |
| spl id | 41371183-bf33-3d47-e063-6394a90a094e | id | |
| spl set id | 41371177-2e79-f7b0-e063-6294a90a747a | 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.