Lido King Lidocaine 4% Pain Relieving Gel-Patch

Manufacturer
Galaxy Bio, Inc.
Effective date
2024-10-01
Label type
HUMAN OTC DRUG LABEL
Version
2
Source
full-release
Hydrated at
2026-06-01 01:29:04

Label at a glance#

ProductLido King Lidocaine 4% Pain Relieving Gel-Patch
Active ingredientLIDOCAINE
Label structure9 sections

Indications and uses

For temporary relief of pain

Dosage and administration

Adults and children 12 years of age and over: clean and dry affected area remove film from patch and apply to the skin (see illustration) apply to affected area not more than 3 to 4 times daily remove patch from the skin after at most 8-hour application Children under 12 years of age: consult a doctor

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Purpose

OTC - PURPOSE SECTION

Topical anesthetic

Uses

INDICATIONS & USAGE SECTION

For temporary relief of pain

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • if you are allergic to any ingredients of this product
  • more than one patch at a time
  • on wounds or damaged skin
  • with a heating pad
  • if pouch is damaged or opened

When using this product

OTC - WHEN USING SECTION

  • avoid contact with the eyes, mucous membranes or rashes
  • use only as directed
  • do not bandage tightly
  • do not reuse patch

Stop use and ask a doctor if

OTC - STOP USE SECTION

  • localized skin reactions occur, such as rash, itching, redness, irritation, pain, swelling and blistering
  • symptoms clear up and occur again within a few days
  • symptoms persist for more than 7 days
  • conditions worsen

If pregnant or breast-feeding,

OTC - PREGNANCY OR BREAST FEEDING SECTION

ask a health professional before use.

Keep out of reach of children.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact a Poison Control Center right away.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over:

  • clean and dry affected area
  • remove film from patch and apply to the skin (see illustration)
  • apply to affected area not more than 3 to 4 times daily
  • remove patch from the skin after at most 8-hour application

Children under 12 years of age: consult a doctor

Other information

OTHER SAFETY INFORMATION

  • store in a cool dry place
  • protect product from freezing, excessive heat and moisture
  • avoid storing product in direct sunlight

Inactive ingredients

INACTIVE INGREDIENT SECTION

dihydroxyaluminum aminoacetate, edetate disodium, glycerin, kaolin, methylparaben, polyacrylic acid, propylene glycol, propylparaben, polysorbate 80, polyvinylpyrrolidone k90, purified water, sodium polyacrylate, tartaric acid, titanium dioxide

Principal Display Panel

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

CartonCarton

LIDO KING ®

NDC# 73354-1280-2

MAXIMUM

STRENGTH*

LIDOCAINE 4%

Pain Relieving Gel-Patch

Apply for 8 Hours

Designed in USA

Numbing Relief

Good Skin Feel

Unscented

For temporary relief of pain

• Back

• Neck

• Shoulders

• Knees

• Elbows

• Legs

• Arms

5 PATCHES

3 15/16" x 5 1/2" (10 cm x 14 cm)

For Galaxy Bio, Inc.

Cranbury, NJ 08512

Made in China

* Available without a prescription

®Registered Trademark of NAL Pharma

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2263892Lido King 4 % Medicated PatchPSN2
1737778lidocaine 4 % Medicated PatchPSN2
2263892lidocaine 0.04 MG/MG Medicated Patch [Lido King]SBD2
1737778lidocaine 0.04 MG/MG Medicated PatchSCD2
2263892Lido King 4 % Medicated PatchSY2
1737778lidocaine 4 % Medicated PatchSY2

DailyMed Pharmacologic Classes#

Class, Version, Type table
ClassVersionTypeEffective
LIDOCAINE Pharmacologic Class Indexing2Indexing - Pharmacologic Class20180813

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
070fbed5-7088-434a-a7ce-f2a64d8d40acProduct name220260107
bee66ce1-adb7-9d3b-67d9-582e4c54e80fProduct name520250819
860a93dc-4863-49cc-b284-6bbe8191bc48Product name420250214
eaba870a-6a9d-442e-8643-87b3f558a451Product name120250117
9b4cf230-fd05-41d5-98c6-5db9ecb27b86Product name120230117
7d755fa1-1087-4dcd-98f0-6d4bba479a57Product name320210602
f52be47f-7aa7-46c0-b1fa-50c18dd50206Product name120201029
aed701d5-9c75-dfaf-7154-cde46179faeaProduct name920200313
fa8b5901-e681-426f-82fe-54f6d81ec698Product name420180619
332d03e4-aa24-4b11-841a-02bf41081920Product name120171221
c08ab52f-2fc8-4409-9d9f-ed8edc0bd070Product name120171221
68ed98f8-24c2-44a0-944a-6d36e82ce25aProduct name120141222
1cd42bc2-a430-c72b-636d-991b235fbf80Product name120140508
49fa150c-f0de-cce7-3d9c-993ed81c5698Product name120140508
4d7ae718-ed00-bae8-2abe-9eaec1eef7ffProduct name120140508
9137811f-f279-8640-5aeb-99fa2145d64dProduct name120140508

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
73354-1280-2Lido King Lidocaine 4% Pain Relieving Gel-Patch1 g in 1 PATCHPATCH12
73354-1280-2Lido King Lidocaine 4% Pain Relieving Gel-Patch5 in 1 CARTONPATCH52

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73354-128073354-1280-2

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 15 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
Lido King Lidocaine 4% Pain Relieving Gel-PatchLIDOCAINEGalaxy Bio, Inc.2243734a-4ea2-a5e5-e063-6294a90aba152024-10-01WarningsExact identifier
ndc (package): 73354-1280-2
ndc (product): 73354-1280
ndc11 (package): 73354128002
spl id: 236362ce-50c3-7aee-e063-6394a90a580f
spl set id: 2243734a-4ea2-a5e5-e063-6294a90aba15

Reported adverse events (FAERS/openFDA)#

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