FDA label 470548f7-bbeb-1507-e063-6394a90a4ff8

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
be549228-dfec-489f-973e-af057f7c114d
SPL ID
470548f7-bbeb-1507-e063-6394a90a4ff8
Version
2
Effective date
2025-12-28
Source export date
2026-10-12
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/2026-10-12/b939c18fdf51df171cf60ce5558819d08ac66bb16bb9991d48cbec91028d783e/drug-label-0004-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:38:34

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 Do not use if seal on snap-on lid is broken or missing. Stop use and ask a doctor if symptoms persist for more than 7 days or worsen. As with any drug, ask a doctor before use if pregnant or nursing. Keep this and all medications out of the reach of children. In case of emergency or accidental overdose, contact a medical professional or a Poison Control Center immediately.

Reported adverse events (FAERS/openFDA)#

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