FDA label f6555c5a-f43b-4178-b78a-42dcdb9c4618

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: 6487e3e4-2e2c-4383-aad6-277d156f363e
SPL ID: f6555c5a-f43b-4178-b78a-42dcdb9c4618
Version: 1
Effective date: 2013-08-02
Source export date: 2026-10-22
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/2026-10-22/e5f4d4a4616a7a32d70e04156e4d0babf78b8f6273b85bc55228fdc2c537c220/drug-label-0005-of-0014.json.zip
Source manifest SHA-256: 5de9d3c3492926d1703b492ae4d29b036ac5be73edfcb92a6cd5eb95a2acef9c
Import run: 20261023T001338Z
Imported at: 2026-10-23 00:38:49

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		f6555c5a-f43b-4178-b78a-42dcdb9c4618	id
spl set id		6487e3e4-2e2c-4383-aad6-277d156f363e	set_id

openFDA text is shown for search and cross-checking; DailyMed SPL is canonical.

Warnings sections page 1 of 1 · 1 matching rows.

If no improvement is seen after 7 days or new symptoms develop, discontinue use.

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