FDA label 219a2d6b-3a9a-4613-8fdf-e21360ad9add

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
ecc419e9-a89d-4c5d-988f-3d646779d959
SPL ID
219a2d6b-3a9a-4613-8fdf-e21360ad9add
Version
1
Effective date
2019-09-15
Source export date
2026-11-06
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/2026-11-06/d05434af5edc4383b7c7894a8f2d94df21171d17714450933cecdfc35cedfa3d/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 06:44:56

Warnings cross-check#

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

Warnings sections page 1 of 1 · 2 matching rows.

warnings

Warnings For external use only

warnings and cautions

Caution Discontinue use if excessive irritation of the skin develops Avoid contact with the eyes and mucous membranes Arthritis: if pain persists for more than 10 days, or redness is present, or in conditions affecting children under 12 years of age consult a physician immediately

Reported adverse events (FAERS/openFDA)#

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