Lidoxi

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)

Brand name
Lidoxi
Generic name
LIDOCAINE
Manufacturer
T&T Pharma Holdings LLC
Product type
HUMAN OTC DRUG
SPL set ID
513c517e-c098-02aa-e063-6294a90ac8a4
SPL ID
513c517e-c099-02aa-e063-6294a90ac8a4
Version
1
Effective date
2026-05-07
Source export date
2026-09-28
Source partition
6
Source file
https://download.open.fda.gov/drug/label/drug-label-0006-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/e0861bcde1444ef952820955caafc6f3fd29783e5ade07a13d933aa3336b399f/drug-label-0006-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:36:13
Harmonized routes table
Harmonized routes
CUTANEOUS

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 Allergy Alert Local anesthetics may cause methemoglobinemia. If an allergic reaction occurs, stop use and seek medical attention immediately. Do Not Use - On damaged, irritated, or infected skin - With a bandage or heating pad - If you are allergic to any ingredients in this product - In the eyes, nose, or mouth - Otherwise as directed When Using This Product Avoid contact with the eyes, nose, and mouth Stop Use and Ask Doctor If - Any of the Warnings apply to you - Excessive skin irritation develops - Condition worsens - Symptoms persist for more than 7 days, or symptoms clear up and occur aqain within 3 days If Pregnant or Breast-feeding Ask a healthcare professional before use Keep Out of Reach of Children If ingested seek medical help or contact a Poison Control Center immediately Flammable Keep away from excessive heat or open flame

Reported adverse events (FAERS/openFDA)#

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