FDA.reportPublic FDA data

FDA label f820ca4e-b093-bd2e-e053-6394a90a6ff1

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
9ad8885f-e450-43ad-964f-e63cd9c041d5
SPL ID
f820ca4e-b093-bd2e-e053-6394a90a6ff1
Version
9
Effective date
2023-03-30
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 05:43:24

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. Avoid contact with the eyes. If contact occurs, rinsethoroughly with cool water. In case of ingestion call Poison Control or contact your physician. Do not use: on open wounds, cuts, infected skin, mouth, genitals, or mucous membranes. Do not use: if you are allergic to any other type of numbing medication. Do not use: if taking Class I antiarrhythmic drugs (such as Tocainide and Mexiletine). Consult your physician for children under 13 years.

Reported adverse events (FAERS/openFDA)#

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