FDA label d58d3575-cc23-bfc6-e053-2995a90afa6b

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
08f4bb41-9cde-4022-af6e-971eca87adc8
SPL ID
d58d3575-cc23-bfc6-e053-2995a90afa6b
Version
2
Effective date
2022-01-14
Source export date
2026-10-12
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/fb14b8f3d34b45230a84f851c029385f512adf3f002423a9b78d4f7ca626ecec/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:20:34

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 • 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 breastfeeding, • consult physician prior to use.

Reported adverse events (FAERS/openFDA)#

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