Home FDA labels 0dd152b5-cad6-4961-9d83-eb39bef68bc0 FDA label 0dd152b5-cad6-4961-9d83-eb39bef68bc0 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 f1d86a82-95e2-4bd6-97c4-a0b60dd2b89c
SPL ID 0dd152b5-cad6-4961-9d83-eb39bef68bc0
Version 2
Effective date 2019-12-24
Source export date 2026-10-12
Source partition 13
Source file https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256 7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run 20261013T011858Z
Imported at 2026-10-13 03:03:28 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.
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 If symptoms worsen or persist for more than 7 days seek advice of physician. If pregnant or breastfeeding consult a healthcare professional before use. Keep out of reach of children. Contains alcohol: In case of accidental overdose, consult a poison control center immediately.
Reported adverse events (FAERS/openFDA)# Adverse event summaries are temporarily unavailable. Other product information remains available.