FDA label 2a1793fd-ffbe-4170-8cb0-32ec9485635b

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: 9cc2db6f-70eb-4207-b831-34fb1e3bb5af
SPL ID: 2a1793fd-ffbe-4170-8cb0-32ec9485635b
Version: 4
Effective date: 2013-03-13
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 02:06:09

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		2a1793fd-ffbe-4170-8cb0-32ec9485635b	id
spl set id		9cc2db6f-70eb-4207-b831-34fb1e3bb5af	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

For external use only Avoid contact with eyes If symptoms persist for more than seven days, or clear up and occur again within a few days, discontinue use and consult physician If redness, irritation, swelling, pain or ot5her symptoms increase, discontinue use and consult physician If swallowed consult physician.

Reported adverse events (FAERS/openFDA)#

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