007

Manufacturer
Shenzhen Chaoxiji Technology Co.,Ltd.
Effective date
2026-08-27
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-01 13:02:15

Label at a glance#

Product4% Lidocaine Patches
Active ingredientLIDOCAINE
Label structure12 sections

Dosage and administration

Adults and children 12 years of age and over: Clean and dry affected area.Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Use one patch for up to 12 hours. Discard patch after single use.Children under 12 years of age: consult a physician.

Storage and handling

Store in a clean, dry place outside of direct sunlight. Protect product from excessive moisture.

Label contents#

Full prescribing information#

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4.0%

Purpose

OTC - PURPOSE SECTION

Topical Anesthetic

Use

INDICATIONS & USAGE SECTION

Temporarily relieves minor pain.

Warnings

WARNINGS SECTION

For external use only

When using this product

OTC - WHEN USING SECTION

▪Use only as directed

▪Read and follow all directions and warnings on this carton

▪Do not allow contact with the eyes DO not use at the same time as other topical analgesics

▪Do not bandage tightly or apply local heat (such as heating pads) to the area of use

▪ Dispose of used patch in a 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.

Do not use

OTC - DO NOT USE SECTION

▪More than one patch on your body at a time

▪On cut, irritated or swollen skin

▪On puncture wounds

▪For more than one week without consulting a doctor

▪If you are allergic to any active or inactive ingredients

▪If pouch is damaged or opened.

Stop use and consult a doctor if

OTC - STOP USE SECTION

▪Condition worsens

▪Redness is present

▪Irritation develops

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

▪You experience signs of skin injury, such as pain, swelling or blistering where the product was applied.

If pregnant or breastfeeding, ask a health professional before use.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children and pets.

Directions

DOSAGE & ADMINISTRATION SECTION

Adults and children 12 years of age and over: Clean and dry affected area.Carefully remove backing from patch starting at a corner. Apply sticky side of patch to affected area. Use one patch for up to 12 hours. Discard patch after single use.Children under 12 years of age: consult a physician.

Other information

STORAGE AND HANDLING SECTION

Store in a clean, dry place outside of direct sunlight. Protect product from excessive moisture.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Aluminum Glycinate, Aluminum Hydroxide, Cellulose Gum, DMDM Hydantoin, Glycerin, Polyacrylic Acid, Polysorbate 80, Propylene Glycol, Ricinus Communis Seed Oil (castor), Silica, Sodium Polyacrylate, Tartaric Acid, Titanium Dioxide, Urea, Water

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Package Label:

87794-007-0187794-007-01

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
87794-00787794-007-01

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
4% Lidocaine Patches4% LIDOCAINE PATCHESShenzhen Chaoxiji Technology Co.,Ltd.5a16c6aa-3ab0-3e46-e063-6294a90a6d8f2026-08-27WarningsExact identifier
ndc (package): 87794-007-01
ndc (product): 87794-007
ndc11 (package): 87794000701
spl id: 5a16c6b7-465d-3fab-e063-6294a90a58d0
spl set id: 5a16c6aa-3ab0-3e46-e063-6294a90a6d8f

Reported adverse events (FAERS/openFDA)#

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