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
2026-09-28
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 05:13:45

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.