Treatonic LIDOCAINE PAIN RELIEF

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
Treatonic LIDOCAINE PAIN RELIEF
Generic name
LIDOCAINE 4%
Manufacturer
100 KARMA INC
Product type
HUMAN OTC DRUG
SPL set ID
3bd66b03-ac82-2d45-e063-6294a90a610a
SPL ID
3bd66b03-ac83-2d45-e063-6294a90a610a
Version
1
Effective date
2025-08-08
Source export date
2026-09-28
Source partition
8
Source file
https://download.open.fda.gov/drug/label/drug-label-0008-of-0014.json.zip
Source object key
raw/openfda/drug-label/2026-09-28/ae3816359e336a5de4f44607730a3d12ceb61ffa012a132189ceda22541b38ee/drug-label-0008-of-0014.json.zip
Source manifest SHA-256
cd2e66336a5cd2223fa3995098fdbdb84c6a7ee5c0a4addb236ccb22dd1e6887
Import run
20260929T050834Z
Imported at
2026-09-29 05:54:20
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

For external use only more than one patch on your body at a time on cut, irritated or swollenskin on puncture wounds for more than one week without consulting a doctor if you are allergic to any active or inactive ingredients if pouch is damaged or opened use only as directed read and follow all directions and warnings on this carton do not allow contact with the eyes do not use at the same time with other topical analgesics do not bandage tightly or apply local heat (such asheating pads) to the area ofuse, do not microwave dispose of used patch in amanner that always keeps product away from children and pets used patches still contain drug product that can produce serious adverse effects if a child or pet chews or ingests this patch. condition worsens redness is present irritation develops symptoms persist for more than 7 days or clear up and occur again within a few days develop signs of skin injury, including pain, swelling, or blistering where the product was applied, ask a health professional before use In case of accidental ingestion, seek medical advice immediately or contact a Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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