FDA.reportPublic FDA data

FDA label f2797fbd-ee5e-484e-e053-2995a90aba1a

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
a0be67e3-742b-0bfd-e053-2995a90a976b
SPL ID
f2797fbd-ee5e-484e-e053-2995a90aba1a
Version
5
Effective date
2023-01-17
Source export date
2026-08-01
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-08-01/206e0852f7011b53c21719ec5c68ac6752381d0fcd1d348f7428adad64429e89/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
bdd1454d0606b622b70458a306b8a10d8a8787db06fd9f46e69c7f7a4524b630
Import run
20260801T225920Z
Imported at
2026-08-01 23:17:34

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 this product except under the advice and supervision of a doctor. Do not use if bottom ridge of tube cap is exposed. To avoid contamination, do not touch tip of container to any surface. Replace cap after using. May cause temporary burning and irritation upon application into the eye.