FDA label 43d3bd70-9922-a7e6-e063-6394a90a90ef

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: f037a079-fdbd-3588-e053-2995a90a6621
SPL ID: 43d3bd70-9922-a7e6-e063-6394a90a90ef
Version: 3
Effective date: 2025-11-17
Source export date: 2026-09-28
Source partition: 10
Source file: https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 06:08:50

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		43d3bd70-9922-a7e6-e063-6394a90a90ef	id
spl set id		f037a079-fdbd-3588-e053-2995a90a6621	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. If pregnant or breast feeding • If pregnant or breast feeding, ask a health professional before use. KEEP OUT OF REACH OF CHILDREN • Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. Stop use and ask a doctor if Stop use and ask a doctor if: • You experience eye pain, changes in vision, continued redness or irritation of the eye. • The condition worsens or persists for more than 72 hours.

Reported adverse events (FAERS/openFDA)#

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