FDA label 43d27834-926e-302b-e063-6394a90a18af

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: f03a9f93-d6cb-f5d9-e053-2a95a90a4d83
SPL ID: 43d27834-926e-302b-e063-6394a90a18af
Version: 3
Effective date: 2025-11-17
Source export date: 2026-10-12
Source partition: 7
Source file: https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:03:00

Harmonized identifier links#

Every typed identifier imported from the complete openFDA harmonization object is paginated here; values are not reduced to a first match.

Harmonized identifiers page 1 of 1 · 2 matching rows.

Type, Scope, Identifier table
Type	Scope	Identifier	Source field
spl id		43d27834-926e-302b-e063-6394a90a18af	id
spl set id		f03a9f93-d6cb-f5d9-e053-2a95a90a4d83	set_id

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 use in eyes only. Retain outer carton for full product drug facts. For external use only. To avoid contamination, do not touch tip of container to any surface. Keep tube tightly closed. Stop use and ask a doctor Stop use and ask a doctor if : You experience eye pain, changes invision, continued redness or irritation of the eye. The condition worsens or persists for more than 72 hours. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. If pregnant or breast feeding 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.