FDA.reportPublic FDA data

FDA label f42ac0ee-2d86-1dfb-e053-2995a90aa656

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
ec7944f0-3a46-45c7-81d1-1d828e857456
SPL ID
f42ac0ee-2d86-1dfb-e053-2995a90aa656
Version
2
Effective date
2023-02-08
Source export date
2026-08-01
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/63703fa640102c69d41ceeb8d73f46d0a0be448587814b2aeca60b43bed7e054/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:37:32

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 Do not use except under the advice and supervision of a doctor When using this product • It may cause temporary burning and irritation • Replace cap after use • To avoid contamination do not touch tip of container to any surface. Stop use and ask a doctor if • Condition worsens or persists for more than 72 hours. • You experience eye pain, changes in vision, continued redness or irritation of the eye Keep out of the reach of children. If swallowed, get medical help or contact a Poison Control Center right away.