83559-019

Manufacturer
Henan Enokon Medical Instrument Co., Ltd.
Effective date
2026-07-29
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-07-31 05:10:23

Label at a glance#

ProductAuixudin Lidocaine Pain Relief Gel-Patch
Active ingredientLIDOCAINE
Label structure13 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 1 patch at a time to affected area, not more than 3 to 4 times daily *remove patch from the skin after at most 8 hours of application

Storage and handling

*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%

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

*more than 1 patch at a time
*on wounds or damaged skin
*with a heating pad
*if you have ever had an allergic reaction to this product or any of its ingredients

When Using

OTC - WHEN USING SECTION

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

Stop Use

OTC - STOP USE SECTION

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

Ask Doctor

OTC - ASK DOCTOR SECTION

*If pregnant or breast-feeding, ask a health professional before use.
*Children under 12 years of age: Consult a doctor

Keep Out Of Reach Of Children

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If swallowed, get medical help or contact with 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 1 patch at a time to affected area, not more than 3 to 4 times daily
*remove patch from the skin after at most 8 hours of application

Other information

STORAGE AND HANDLING SECTION

*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,Edetate Disodium,Ethylhexylglycerin,Glycerin,Kaolin,Phenoxyethanol,Polyvinylpyrrolidone,Propylene Glycol,Sodium Carboxymethylcellulose,Sodium Polyacrylate,Tartaric Acid,Water

PRINCIPAL DISPLAY PANEL

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

5Patch5Patch40Patch40Patch

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
BarcodeEAN-136974159744143GTIN-13: 6974159744143
EAN-13: 6974159744143
GTIN storage (14 digits): 06974159744143
40Patch.jpg
QR code linkQR Codeqr21.cn/DPO2j040Patch.jpg, 5Patch.jpg

Products#

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

DailyMed product names page 1 of 1 · 15 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
83559-01983559-019-01, 83559-019-02

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 13 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
Auixudin Lidocaine Pain Relief Gel-PatchLIDOCAINE PAIN RELIEF GEL-PATCHHenan Enokon Medical Instrument Co., Ltd.57bc7b9e-e2f7-724b-e063-6394a90ab36f2026-07-29WarningsExact identifier
ndc (package): 83559-019-02
ndc (package): 83559-019-01
ndc (product): 83559-019
ndc11 (package): 83559001901
ndc11 (package): 83559001902
spl id: 57bc7b9e-e2f8-724b-e063-6394a90ab36f
spl set id: 57bc7b9e-e2f7-724b-e063-6394a90ab36f

Reported adverse events (FAERS/openFDA)#

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