FDA label 291a6b5a-f18b-416c-e063-6294a90a090c

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: b3e55f57-3d9d-2a0e-e053-2995a90a4c58
SPL ID: 291a6b5a-f18b-416c-e063-6294a90a090c
Version: 8
Effective date: 2024-12-12
Source export date: 2026-11-06
Source partition: 4
Source file: https://download.open.fda.gov/drug/label/drug-label-0004-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-11-06/b00a73f24c6ff050408c570063640e3d80d1f71dfc9a165d1cf072a25659445a/drug-label-0004-of-0014.json.zip
Source manifest SHA-256: 4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run: 20261108T063105Z
Imported at: 2026-11-08 07:02:03

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		291a6b5a-f18b-416c-e063-6294a90a090c	id
spl set id		b3e55f57-3d9d-2a0e-e053-2995a90a4c58	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 external use only.When using this product • Do not get into eyes Stop use and ask a doctor if• Conditions worsens• symptoms last more than 7 days or clear up and occur again within a few days. - In case of accidental ingestion, contact a physician or a Poison Control Center immediately. When using this product When using this product Do not get into eyes Stop use and ask a doctor if Stop use and ask a doctor if• Conditions worsens• symptoms last more than 7 days or clear up and occur again within a few days. - In case of accidental ingestion, contact a physician or a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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