Active ingredient

Manufacturer
ZHI Technologies, Inc.
Effective date
2026-09-03
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
daily-update
Hydrated at
2026-09-08 02:02:20

Label at a glance#

ProductZHI Technologies
Active ingredientLIDOCAINE, MENTHOL
Label structure6 sections

Indications and uses

For the temporary relief of pain

Dosage and administration

Adults and children 12 years of age and older: Clean and dry affected area Press patch firmly onto affected area after removing the clear plastic lining. The patch has a lasting effect of up to 24 hours and should be worn continuously. Use one patch at a time and not more than 3 to 4 times daily Children under 12 years of age: consult a doctor.

Label contents#

Full prescribing information#

Active ingredient

OTC - ACTIVE INGREDIENT SECTION

Lidocaine 4% 

Menthol 1%

Uses

INDICATIONS & USAGE SECTION

For the temporary relief of pain

Warning

WARNINGS SECTION

  • For external use only.

Don’t use

  • on punctured, cut, irritated, damaged, or swollen skin.
  • More than one patch on your body at a time or with other topical analgesics at the same time.
  • With a heating pad or apply local heat to the area of the use

When using this Product

  • Use on as directed
  • Do not bandage tightly
  • Avoid 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 a manner that keeps product away from children and pets (used patches still contain drug product that can produce serious adverse effects if a child or pet chews or ingests the patch).

Stop use and ask a doctor if:

  • Your condition worsens or symptoms persist for more than 7 days.
  • Your symptoms clear up and then occur again within a few days.
  • You have severe burning, redness, or irritation.
  • 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.

Keep out of reach of children and pets. 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 older:

Clean and dry affected area

Press patch firmly onto affected area after removing the clear plastic lining. The patch has a lasting effect of up to 24 hours and should be worn continuously.

Use one patch at a time and not more than 3 to 4 times daily

Children under 12 years of age: consult a doctor.

Inactive ingredients

INACTIVE INGREDIENT SECTION

Adhesive, mineral oil.

Product label

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

image descriptionimage descriptionimage descriptionimage description

Product Linked Resources#

Resource, Code type, Value table
ResourceCode typeValueEquivalent identifiersSource image
QR code linkQR Codezhitechnologies.com/image_002.jpg

Products#

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

DailyMed product names page 1 of 1 · 6 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
87965-00187965-001-01, 87965-001-02, 87965-001-03

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 4 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
ZHI TechnologiesLIDOCAINE, MENTHOLZHI Technologies, Inc.6717e995-4d2d-49e8-8ecf-7c62557dfdef2026-09-03WarningsExact identifier
ndc (package): 87965-001-03
ndc (package): 87965-001-02
ndc (package): 87965-001-01
ndc (product): 87965-001
ndc11 (package): 87965000101
ndc11 (package): 87965000102
ndc11 (package): 87965000103
spl id: 5a9b286f-a68d-df85-e063-6294a90aad61
spl set id: 6717e995-4d2d-49e8-8ecf-7c62557dfdef

Reported adverse events (FAERS/openFDA)#

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