FDA label 07069d90-f43f-a4c8-e063-6294a90ad390

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
f2b463d7-3fcf-4b2c-8ba2-8e51e3290de2
SPL ID
07069d90-f43f-a4c8-e063-6294a90ad390
Version
3
Effective date
2023-10-06
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 06:45:15

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, or clear up and occur again within a few day, discontinue use and consult physician. - If redness, irritation, swelling, pain or other symptoms increase, discontinue use and consult physician. - Keep out of reach of children. If swallowed, consult physician.

Reported adverse events (FAERS/openFDA)#

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