FDA label fe43061a-be2e-e873-e053-6294a90adbe3

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
fdb74c89-255d-ab2b-e053-6294a90a098b
SPL ID
fe43061a-be2e-e873-e053-6294a90adbe3
Version
2
Effective date
2023-06-16
Source export date
2026-10-12
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/2026-10-12/befa34274042a52f589b22fe2add0b1c6f0a385c96447c28303de164bb144af5/drug-label-0010-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 02:30:57

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. Before using this product perform an allergy test by applying a small amount of product on the forearm. If no side effect appear after 30 minutes, such asredness, irritation or itching, you can start applying it. Keep out of the reaching of children The use of this product has not been tested in areas such as eyes contours and mucus membranes. Do not use if allergic to lidocaine or other local anesthetics For all kind of skin If any side effect is observed, discontinue use and consult your healthcare practicioner

Reported adverse events (FAERS/openFDA)#

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