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
2026-10-12
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 - 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.