FDA.reportPublic FDA data

FDA label 0749330b-1725-5d6b-e063-6394a90a3f5e

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 (canonical bytes are SHA-256 checked before publication)

SPL set ID
a1d90bb4-37d1-4953-8146-0e28f14b6f17
SPL ID
0749330b-1725-5d6b-e063-6394a90a3f5e
Version
4
Effective date
2023-10-09
Source export date
2026-10-12
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/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:39

Warnings cross-check#

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings: • Always consult a physician before use. • For external use only. • Avoid contact with eyes. • If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. • If swallowed, consult physician. • Do not apply to wounds or damaged skin. • Do not bandage tightly. If pregnant or breast feeding, ask a health professional before use. Allergy Alert: If you have had a prior allergic reaction to aspirin or salicylates, please consult physician prior to use.

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.