Lido King

Manufacturer
Galaxy Bio, Inc.
Effective date
2020-04-13
Label type
HUMAN OTC DRUG LABEL
Version
3
Source
legacy-cache
Hydrated at
2026-08-01 22:10:57

Label at a glance#

ProductLido King
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: • cut to desired size, if necessary • 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:

  • cut to desired size, if necessary
  • 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 at 68°-77°F (20°-25°C)
  • 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, polyvinyl alcohol solution, propylene glycol, propylparaben, purified water, sodium carboxymethylcellulose, sodium polyacrylate, sodium polyacrylate starch, sorbitol solution, tartaric acid, urea

Questions or comments?

OTC - QUESTIONS SECTION

Toll free 1-833-525-0303  www.lidokingpatch.com

SPL UNCLASSIFIED SECTION

For Galaxy Bio, Inc.

Monmouth Junction, NJ 08852

Made in Taiwan

*Available without a prescription

® Registered Trademark

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

NEW

APPLY FOR

8

HOURS

LIDO KING ®

LIDOCAINE 4%

Pain Relieving Gel-Patch

Maximum Strength*

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)

NDC: 73354-1279-2

Lido King (Lidocaine 4%) labelLido King (Lidocaine 4%) label

FDA-Initiated Inactive NDC Indexing#

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
73354-1279LIDO KING (LIDOCAINE) PATCH [GALAXY BIO, INC.]3Legacy NDC20220129_329bac8a-7f4a-4be4-95ec-1e578c45e677.zip

DailyMed Billing Units#

Package NDC, Billing unit, Product NDC table
Package NDCBilling unitProduct NDCDailyMed indexing SPLSPL versionEffective
73354-1279-2EA - Each73354-127966a9b61f-07a2-4b6d-b16d-03c58bb697c112020-01-03

Products#

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

DailyMed product names page 1 of 1 · 17 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
73354-127973354-1279-2

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 16 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
472e9196-1304-7cca-e063-6394a90a8ba3329bac8a-7f4a-4be4-95ec-1e578c45e6772025-12-30WarningsExact identifier
spl set id: 329bac8a-7f4a-4be4-95ec-1e578c45e677

Reported adverse events (FAERS/openFDA)#

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