FDA label e8491335-6eff-630d-e053-2995a90ae956

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
e4c7d942-e37c-492c-9160-3223995007c3
SPL ID
e8491335-6eff-630d-e053-2995a90ae956
Version
3
Effective date
2022-09-09
Source export date
2026-09-28
Source partition
10
Source file
https://download.open.fda.gov/drug/label/drug-label-0010-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/4bbc9760f647649b787710953d978bd6419e899ba8b90f32c3d972aae43947f8/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 06:09:48

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 in large quantities, particularly over raw surfaces or blistered areas on puncture wounds if you are allergic to lidocaine or any of the inactive ingredients When using this product use only as directed avoid contact with eyes. Stop use and ask a doctor if allergic reaction occurs condition worsens or if symptoms persist for more than 7 days symptoms clear up and return within a few days redness, irritation, swelling, pain or other symptoms begin or increase If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children and pets. If ingested, get medical help or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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