Lidocare Arm, Neck, Leg

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
Lidocare Arm, Neck, Leg
Generic name
4% LIDOCAINE
Manufacturer
Kingsway Pharmaceuticals dba NFI, LLC
Product type
HUMAN OTC DRUG
SPL set ID
59a104ee-7034-99c3-e053-2991aa0a164c
SPL ID
509ddde0-40b2-4440-991b-37523ad55812
Version
6
Effective date
2025-01-06
Source export date
2026-10-12
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/2026-10-12/ff22b88bd32e56cbc369af80345075227138a42b1b3ba9a84f038fd5493a7a47/drug-label-0007-of-0014.json.zip
Source manifest SHA-256
7e6b178df8f32cac9a78e0f5d09c588344509b04fe41effb1dde9102e2a45be6
Import run
20261013T011858Z
Imported at
2026-10-13 01:56:13
Harmonized routes table
Harmonized routes
TOPICAL

Warnings cross-check#

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Warnings sections page 1 of 1 · 1 matching rows.

warnings

Warnings For external use only. Do not use if pouch is damaged or opened. Do not use • on large areas of the body or on cut, irritated skin • on open wounds or sensitive skin • for more than one week without consulting a doctor • do not use if you are allergic to lidocaine or any of the inactive ingredients listed below. When using this product • use only as directed. Read and follow all directions and warnings on this package. • do not allow contact with the eyes • do not bandage or apply local heat (such as heating pads) to the area of use • do not reuse patch. Stop use and ask doctor if • condition worsens • rash, itching or skin irritation develops • symptoms persist for more than 7 days or clear up and occur again within a few days If pregnant or breast feeding, ask a health professional before use. Keep out of reach of children and pets. If swallowed, get medical help or contact Poison Control Center right away.

Reported adverse events (FAERS/openFDA)#

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