FDA label ec5c3b88-f79e-cdd6-e053-2995a90a8c08

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
26bba135-758f-4315-9e37-bc29300ccafd
SPL ID
ec5c3b88-f79e-cdd6-e053-2995a90a8c08
Version
4
Effective date
2022-10-31
Source export date
2026-10-12
Source partition
4
Source file
https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:36:32

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 USE ONLY AS DIRECTED WHEN USING THIS PRODUCT avoid contact with eyes ask you doctor to check your INR more frequently if you are taking anticoagulants DO NOT USE do not use if you are allergic to salicylates, aspirin, or any of the inactive ingredients do not use if seal is broken or is not visible Stop use and ask a doctor if condition worsens redness is present irritation develops symptoms persist for more than 7 days or clear up and occur again within a few days keep out of reach of children If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding ask a health professional before use.

Reported adverse events (FAERS/openFDA)#

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