FDA label 4488ff62-8f05-42a3-b175-5fb81db8a008

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: fd531891-7a29-4b1b-86c4-b69264cc5777
SPL ID: 4488ff62-8f05-42a3-b175-5fb81db8a008
Version: 1
Effective date: 2011-06-01
Source export date: 2026-10-12
Source partition: 12
Source file: https://download.open.fda.gov/drug/label/drug-label-0012-of-0014.json.zip
Source object key: raw/openfda/drug-label/2026-10-12/edd23646015c9adc800cdbe2b778398a2d2b70e90dce5721ef2b191499a0397f/drug-label-0012-of-0014.json.zip
Source manifest SHA-256: 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run: 20261013T011858Z
Imported at: 2026-10-13 02:49:42

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		4488ff62-8f05-42a3-b175-5fb81db8a008	id
spl set id		fd531891-7a29-4b1b-86c4-b69264cc5777	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 symptoms persist, consult a physician. Do not use if ring on bottom of cap is broken or missing.

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