FDA.reportPublic FDA data

FDA label 298ef877-b9b6-01ac-e063-6394a90a44b5

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
faf55940-2121-ec0a-e053-6394a90afa8a
SPL ID
298ef877-b9b6-01ac-e063-6394a90a44b5
Version
3
Effective date
2024-12-18
Source export date
2026-11-06
Source partition
9
Source file
https://download.open.fda.gov/drug/label/drug-label-0009-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-11-06/5731a8c92e1c0dd2a09d2f92b410e7a70ea29cbf6b8040a6a05e4be5b7c51f0d/drug-label-0009-of-0014.json.zip
Source manifest SHA-256
4a7570ba105b5a039a8e1c94a85e7f085b9047a8882a35a96bf1e4516c5ffc97
Import run
20261108T063105Z
Imported at
2026-11-08 07:44:37

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 Do not use if you are allergic to any of the ingredients in the eyes over large areas of the body Ask a doctor before use if you have deep or puncture wounds, serious burns, animal bites Stop use and ask a doctor if you need to use longer than 1 week the condition persists or gets worse rash or other allergic reaction develops Keep out of reach of children If swallowed, get medical help or contact a Poison Control Center (1-800-222-1222) right away. When using this product use as directed

Reported adverse events (FAERS/openFDA)#

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