AUVON LIDOCAINE MENTHOL Pain Relief

Manufacturer
SHENZHEN YUWEN E-COMMERCE CO., LTD.
Effective date
2024-12-05
Label type
HUMAN OTC DRUG LABEL
Version
5
Source
full-release
Hydrated at
2026-06-01 00:41:00

Label at a glance#

ProductAUVON LIDOCAINE MENTHOL Pain Relief
Active ingredientLIDOCAINE, MENTHOL
Label structure9 sections

Dosage and administration

■ Clean and dry the patch application area (no wound or hair), pull to separate the film, peel off one side of the film, apply the exposed patch to the skin, peel off the other side of the film, and press the patch firmly to the skin. ■ Do not repeatedly use or repeatedly reapply the patch as far as possible ■ Cut first if if used on joints ■ Use in te affected area no more than 4 times daily ■ Wash hands with coo...

Storage and handling

Avoid storing patches in direct sunlight Protect patches from excessive moisture

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

AUVON LIDOCAINE MENTHOL Pain Relief Patch

Drug Facts

Active ingredients

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4%

Menthol 1%

Purposes

OTC - PURPOSE SECTION

Topical anesthetic

Topical analgesic

Use

INDICATIONS & USAGE SECTION

for the temporary pain relief

Warnings

WARNINGS SECTION

For external use only

Do not use

OTC - DO NOT USE SECTION

  • If you are allergic to the listed ingredients
  • If you are pregnent or breast feeding
  • If you are under 12 years of age
  • On wounds, cuts, damaged/broken/irritated skin
  • On eyes or mucous membranes 
  • With heating pads/devices or wrap with a bandage
  • With other topical analgesics
  • If the package arrives damaged or opened.

When using this product

OTC - WHEN USING SECTION

■ Use only as directed

■ Read and follow all directions and warnings on this label

■ avoid contact with the eyes and mucous membranes

■ rare cases of serious burns have been reported with products of this type

■ a transient burning sensation may occur upon application but generally disappears in several days

■ dispose of used patch in manner that always keeps product away from children and pets. Used patches still

contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch.

Stop use and ask a doctor if

OTC - STOP USE SECTION

You are experiencing pain, swelling or blistering

Redness is persent or irritation develops

Symptoms persist for more than 7 days or clear up and occur again within a few days

Keep out of reach of children and pets.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

If ingested, get medical help or contact a Poison Control Center

right away.

Directions

DOSAGE & ADMINISTRATION SECTION

■ Clean and dry the patch application area (no wound or hair), pull to separate the film, peel off one side of the film, apply the exposed patch to the skin, peel off the other side of the film, and press the patch firmly to the skin.

■ Do not repeatedly use or repeatedly reapply the patch as far as possible

■ Cut first if if used on joints

■ Use in te affected area no more than 4 times daily

■ Wash hands with cool water after use

Storage

STORAGE AND HANDLING SECTION

  • Avoid storing patches in direct sunlight
  • Protect patches from excessive moisture

Inactive ingredients

INACTIVE INGREDIENT SECTION

Glycerin, sodium polyacrylate, dihydroxyaluminum aminoacetate,  methylparaben, propylparaben, polyacrylic acid, Kaolin, polysorbate 80, propylene glycol, tartaric acid, PVP, titanium dioxide, water, petrolatum, CMC, mineral oil

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

LabelLabel

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1249758lidocaine 4 % / menthol 1 % Medicated PatchPSN5
1249758lidocaine 0.04 MG/MG / menthol 0.01 MG/MG Medicated PatchSCD5
1249758lidocaine 4 % / menthol 1 % Medicated PatchSY5

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

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
83391-001-012026-01-29C16284748780-149896155-af3a-586f-e063-e6dba90add9083391-001
83391-001-022026-01-29C16284748780-149896155-af3a-586f-e063-e6dba90add9083391-001
83391-001-032026-01-29C16284748780-149896155-af3a-586f-e063-e6dba90add9083391-001

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
83391-001-01AUVON LIDOCAINE MENTHOL Pain Relief1 in 1 CARTONPATCH15
83391-001-02AUVON LIDOCAINE MENTHOL Pain Relief8 in 1 CARTONPATCH85
83391-001-03AUVON LIDOCAINE MENTHOL Pain Relief30 in 1 CARTONPATCH305

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
83391-001AUVON LIDOCAINE MENTHOL PAIN RELIEF (LIDOCAINE AND MENTHOL) PATCH [SHENZHEN YUWEN E-COMMERCE CO., LTD.]53 package rows20241208_9acd645a-9cd8-4030-aba5-ccaaad5eb7da.zip

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
83391-00183391-001-01, 83391-001-02, 83391-001-03

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
28938feb-0cf8-950d-e063-6394a90a7bc19acd645a-9cd8-4030-aba5-ccaaad5eb7da2024-12-05WarningsExact identifier
spl id: 28938feb-0cf8-950d-e063-6394a90a7bc1
spl set id: 9acd645a-9cd8-4030-aba5-ccaaad5eb7da

Reported adverse events (FAERS/openFDA)#

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