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ZHI Technologies drug information

LIDOCAINE, MENTHOL
ZHI Technologies, Inc. · TRANSDERMAL

Product NDC: 87965-001

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Source label information, not individualized medical advice. This record applies to the product and labeler shown below. Compare the exact formulation, strength and country with your package and the current source label.
Generic nameLIDOCAINE, MENTHOL
Labeler / manufacturerZHI Technologies, Inc.
RouteTRANSDERMAL
Drug classAmide Local Anesthetic / Antiarrhythmic
Product NDC87965-001
Label effective date2026-09-03

Official product label reference

ZHI Technologies — ZHI Technologies, Inc.

This page contains 6 source sections for LIDOCAINE, MENTHOL, transdermal route. Label set 6717e995-4d2d-49e8-8ecf-7c62557dfdef, version 1.

Retrieved 2026-10-02 · openFDA dataset updated 2026-10-02 · Check the current DailyMed label

Label records can cover multiple strengths or package sizes. A label listing does not by itself establish FDA approval or current market availability. Check the source and application history for this specific product.

Uses described in the label

Uses For the temporary relief of pain
Dosage and administration — label text
Directions 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.
Warnings
Warning 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.
Active ingredient
Active ingredient Lidocaine 4% Menthol 1%
Child safety
Inactive ingredient
Inactive ingredients Adhesive, mineral oil.

Official sources and product identifiers

Substances listed: LIDOCAINE, MENTHOL

RxNorm identifiers: 1249758

Package NDC codes

87965-001-01, 87965-001-02, 87965-001-03

Further research and background

These are external searches for related information. Research, encyclopedia and news articles have not been imported into this product record.

Coverage and corrections

The text is extracted from a US structured product label. Tables are represented as text where supplied; formatting and illustrations may be lost. A missing section does not mean a risk is absent. This reference has not been independently reviewed by a clinician and is not a live safety-alert service.

Source retrieved 2026-10-02. Read the source policy.