FDA label 121a4f45-0a16-47b2-b65c-82627e592be7

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
7cdef849-0c70-4843-8f6d-ed7377a25ebd
SPL ID
121a4f45-0a16-47b2-b65c-82627e592be7
Version
2
Effective date
2017-11-08
Source export date
2026-10-12
Source partition
1
Source file
https://download.open.fda.gov/drug/label/drug-label-0001-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/7928c8e8c6256620071a8b7e5b93eb8dfa543649c08d17a01ea02251012ba58c/drug-label-0001-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:26:20

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 For external use only. This package is intended for institutional use only. If swallowed, get medical help or contact a Poison Control Center right away. When using this product avoid contact with eyes, not to be applied over deep on puncture wounds, infections or lacerations. Stop use and ask a doctor if condition worsens or does not improve within 7 days.

Reported adverse events (FAERS/openFDA)#

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