FDA label 0722f0a0-7fab-70a6-e063-6394a90a33a6

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
85fe0715-cc17-4676-87cf-2164235745d6
SPL ID
0722f0a0-7fab-70a6-e063-6394a90a33a6
Version
4
Effective date
2023-10-07
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 01:36:49

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. • Avoid contact with eyes. • If symptoms persist for more than seven days, discontinue use and consult physician Keep out of reach of children. If swallowed, consult physician. Do not apply • to wounds or damaged skin. • Do not bandage tightly. If pregnant or breast feeding, • contact physician prior to use.

Reported adverse events (FAERS/openFDA)#

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