FDA label 2d2ead3f-7b6e-4422-b0b3-9139e83aaa77

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
b7fb2184-2563-46f2-82bc-5d9ed4e7c4e6
SPL ID
2d2ead3f-7b6e-4422-b0b3-9139e83aaa77
Version
1
Effective date
2020-02-10
Source export date
2026-09-28
Source partition
5
Source file
https://download.open.fda.gov/drug/label/drug-label-0005-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/9839785a692b692224cd5f90f9e3a9514c9923a6f521ab83eed3bedc7c0e1d05/drug-label-0005-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:31:15

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 If this product, used as directed, does not provide relief, discontinue use and consult a doctor. For topical use only. Do not bandage tightly Do not use if you are allergic to Lidocaine or topical anesthetics. Discontinue use if you develop a rash or irritation, such as burning or itching. If symptoms persist, consult a doctor. Do not use on broken, irritated or sensitive skin. Avoid contact with eyes. For external use only. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center.

Reported adverse events (FAERS/openFDA)#

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