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
- KMM Pharmaceuticals, LLC
- Product type
- HUMAN PRESCRIPTION DRUG
- SPL set ID
- 5df4c5b6-3ad2-7f2c-e053-2991aa0a021b
- SPL ID
- 5df4c5b6-3ad3-7f2c-e053-2991aa0a021b
- Version
- 1
- Effective date
- 2017-11-14
- Source export date
- 2026-09-28
- Source partition
- 1
- Source file
- https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
- Source object key
- raw/openfda/drug-label/2026-09-28/9c7783846d422acb0c9e59457606951c785a7d28cc631c8cc4839d0dc7c55f39/drug-label-0001-of-0014.json.zip
- Source manifest SHA-256
- cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
- Import run
- 20260929T050834Z
- Imported at
- 2026-09-29 05:14:08
| 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 | KMM Pharmaceuticals, LLC | openfda.manufacturer_name | |
| ndc | package | 52187-526-10 | openfda.package_ndc |
| ndc | product | 52187-526 | openfda.product_ndc |
| ndc11 | package | 52187052610 | derived:openfda.package_ndc |
| rxcui | 312887 | openfda.rxcui | |
| spl id | 5df4c5b6-3ad3-7f2c-e053-2991aa0a021b | id | |
| spl set id | 5df4c5b6-3ad2-7f2c-e053-2991aa0a021b | set_id | |
| unii | O414PZ4LPZ | openfda.unii |
Warnings cross-check#
openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.
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.
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.