FDA label 5fc47cf3-56ab-7807-e053-2a91aa0ac541

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: 22a10ee9-d617-3639-e054-00144ff8d46c
SPL ID: 5fc47cf3-56ab-7807-e053-2a91aa0ac541
Version: 3
Effective date: 2017-12-07
Source export date: 2026-09-28
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/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run: 20260929T050834Z
Imported at: 2026-09-29 05:29:41

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		5fc47cf3-56ab-7807-e053-2a91aa0ac541	id
spl set id		22a10ee9-d617-3639-e054-00144ff8d46c	set_id

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. WHEN USING When using this product Do not use in the eyes Discontinue use if irritation or redness develop

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