FDA label c6fea1d0-8c42-90f6-e053-2a95a90aee90

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
81dd93a4-6fc7-cb4a-e053-2a91aa0a3faf
SPL ID
c6fea1d0-8c42-90f6-e053-2a95a90aee90
Version
5
Effective date
2021-07-13
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 01:35:45

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 Avoid contact with eyes Stop use and ask doctor if condition worsen, 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, contact a Poison Control Center right away.

warnings and cautions

Avoid contact with eyes

Adverse reactions cross-check#

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

Adverse reactions sections page 1 of 1 · 1 matching rows.

adverse reactions

to report suspected adverse reactions contact 1-800-332-1088

Reported adverse events (FAERS/openFDA)#

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