FDA label 21a01c8e-a26d-45a8-b238-6c53e7e7ea4a

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
c1c6a20f-d1b1-494d-9762-7b2a95e5421f
SPL ID
21a01c8e-a26d-45a8-b238-6c53e7e7ea4a
Version
1
Effective date
2021-11-04
Source export date
2026-10-12
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/13cbfcd236c665f0ee69e2d9141331148dcdff45d1679c92f029cfba27dd74a2/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:43:18

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 . -------------------------------------------------------------------------------------------------------- When using this product avoid contact with the eyes. In case of contact, flush eyes thoroughly with water -------------------------------------------------------------------------------------------------------- Stop use and ask a doctor if irritation and redness develops and persists.

Reported adverse events (FAERS/openFDA)#

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