FDA label d430049c-16d4-49d1-b053-fecab8db0397

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
9dbcf5b8-8e9a-46f1-ba21-a37137813c32
SPL ID
d430049c-16d4-49d1-b053-fecab8db0397
Version
1
Effective date
2020-02-10
Source export date
2026-10-12
Source partition
13
Source file
https://download.open.fda.gov/drug/label/drug-label-0013-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-10-12/b8dac220ac9fc8ffb4d86c6e00ece30169fc4575ca0cc92e5c9ce1a524fb0249/drug-label-0013-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:59:53

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.