83559-023

Manufacturer
Henan Enokon Medical Instrument Co., Ltd.
Effective date
2026-09-01
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-03 03:03:32

Label at a glance#

ProductGaimoa Lidocaine Pain Relief Gel Patches
Active ingredientLIDOCAINE, MENTHOL
Label structure12 sections

Dosage and administration

Directions Adults and children 12 years of age and over clean and dry affected area 1.remove film from patch and apply to the skin (see illustration) 2.apply 1 patch at a time to affected area, not more than 3 to 4 times daily 3.remove patch from the skin after at most 8 hours of application Children under 12 years of age: Consult a doctor

Storage and handling

Other information avoid storing product in direct sunlight protect product from excessive moisture store at 20-25°C (68-77°F)

Label contents#

Full prescribing information#

Active Ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%
Menthol 1%

Purpose

OTC - PURPOSE SECTION

Topical Analgesic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves muscle soreness and minor joint pain in the wrist, knees, back,neck, hips, shoulders, and elbows.

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

Do not use
1.more than 1 patch at a time
2.on wounds or damaged skin
3.with a heating pad
4.if you have ever had an allergic reaction to this product or any of its ingredients

When Using

OTC - WHEN USING SECTION

When using this product
1.use only as directed
2.avoid contact with the eyes, mucous membranes or rashes
3.do not bandage tightly

Ask Doctor

OTC - ASK DOCTOR SECTION

Children under 12 years of age: consult a doctor

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep Out Of Reach Of Children

Directions

DOSAGE & ADMINISTRATION SECTION

Directions
Adults and children 12 years of age and over
clean and dry affected area
1.remove film from patch and apply to the skin (see illustration)
2.apply 1 patch at a time to affected area, not more than 3 to 4 times daily
3.remove patch from the skin after at most 8 hours of application
Children under 12 years of age: Consult a doctor

Other information

STORAGE AND HANDLING SECTION

Other information
avoid storing product in direct sunlight
protect product from excessive moisture
store at 20-25°C (68-77°F)

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum Glycinate, EdetateDisodium, Ethylhexylglycerin, Glycerin, Kaolin, Phenoxyethanol, Polyvinylpyrrolidone,
Propylene Glycol, Sodium Carboxymethylcellulose, Sodium Polyacrylate, Tartaric Acid, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

11223344556677

Products#

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

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83559-02383559-023-01, 83559-023-02, 83559-023-03, 83559-023-04, 83559-023-05, 83559-023-06, 83559-023-07

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 14 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
Gaimoa Lidocaine Pain Relief Gel PatchesLIDOCAINE PAIN RELIEF GEL PATCHESHenan Enokon Medical Instrument Co., Ltd.5a68fe67-5c15-af9a-e063-6294a90a7ec12026-09-01WarningsExact identifier
ndc (package): 83559-023-02
ndc (package): 83559-023-05
ndc (package): 83559-023-07
ndc (package): 83559-023-04
ndc (package): 83559-023-03
ndc (package): 83559-023-01
ndc (package): 83559-023-06
ndc (product): 83559-023
ndc11 (package): 83559002301
ndc11 (package): 83559002304
ndc11 (package): 83559002306
ndc11 (package): 83559002307
ndc11 (package): 83559002302
ndc11 (package): 83559002303
ndc11 (package): 83559002305
spl id: 5a68fe67-5c16-af9a-e063-6294a90a7ec1
spl set id: 5a68fe67-5c15-af9a-e063-6294a90a7ec1

Reported adverse events (FAERS/openFDA)#

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