FDA label 9d067216-67b7-44f9-8df9-d8378e3c4ce2

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
dd645161-94d0-4b60-b470-273d57e2c68a
SPL ID
9d067216-67b7-44f9-8df9-d8378e3c4ce2
Version
2
Effective date
2022-02-04
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 01:36:46

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. When using this product avoid contact with eyes. In case of eye contact, flush eyes with water. Ask a doctor Stop use and consult a doctor if irritation or redness develops. If condition persists for more than 72 hours, discontinue use. Keep out of reach of children. If product is swallowed, get medical help or contact a Poison Control Center right away. Do not use on children less than 2 months of age or on open skin wounds

Reported adverse events (FAERS/openFDA)#

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