FDA label 298a743f-f2da-3eac-e063-6294a90a77ac

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
acd83722-0141-4831-b599-07eac95acc1e
SPL ID
298a743f-f2da-3eac-e063-6294a90a77ac
Version
3
Effective date
2024-12-18
Source export date
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:55:52

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 do not use if you are allergic to lidocaine or any of the inacitve ingredients listed below When using this product use only as directed. Read and follow all directions and warnings on this carton. do not allow contact with the 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 swallowed, get medical help or contact a Poison Control Center immediately

Reported adverse events (FAERS/openFDA)#

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