FDA.reportPublic FDA data

FDA label 074b4425-6be0-352c-e063-6394a90ac59e

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
550df5b8-52cd-4bca-b19d-f40ce050e893
SPL ID
074b4425-6be0-352c-e063-6394a90ac59e
Version
2
Effective date
2023-10-09
Source export date
2026-09-28
Source partition
7
Source file
https://download.open.fda.gov/drug/label/drug-label-0007-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/bb1af06e95bcf9567b07e56fcf3a03c0cac3c7c82ff89d4c970881174949e5b7/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:43:28

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 not intended for ingestion. When using this product • Avoid contact with eyes Do not use • in large quantities, particularly over raw surfaces or blistered areas Stop use and ask a doctor if symptoms persist for more than seven days. Keep out of reach of children. • If swallowed, get medical help or contact a Poinson Control Center right away. • 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.