ZHI Technologies

ZHI Technologies is an FDA-registered drug product whose active ingredient is LIDOCAINE, MENTHOL. It is labelled by ZHI Technologies, Inc. taken by transdermal and marketed as a human otc drug product. Identifiers on file: NDC 87965-001, application M017, label effective 20260903. It is one of 13 FDA drug label records sharing the active ingredient LIDOCAINE, MENTHOL. This page reproduces the FDA-approved label text so you can check what a product is, who makes it and how it is supplied before discussing it with a pharmacist or prescriber.

Across FDA labelling, products containing LIDOCAINE, MENTHOL are most often described in connection with: temporary relief. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the temporary relief of pain

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.

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.

FDA lists 13 drug label records with LIDOCAINE, MENTHOL as the active ingredient. The most common dosage forms and the manufacturers with the most records are summarised below; strengths, pack sizes and inactive ingredients can still differ between apparently similar products.

What is ZHI Technologies used for?
Uses For the temporary relief of pain

Who makes ZHI Technologies?
ZHI Technologies, Inc. is the labeler of record for ZHI Technologies. 13 FDA label records share the active ingredient LIDOCAINE, MENTHOL, so generic and branded versions may come from different companies; the manufacturer named on your pack is the one that matters for any enquiry.

What form does ZHI Technologies come in?
administered by transdermal. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is ZHI Technologies prescription or over-the-counter?
The FDA label for this product is recorded as human otc drug. Marketing status can differ between strengths and countries, so check the dispensing rules where you live.

Are there other products containing LIDOCAINE, MENTHOL?
Yes. 13 FDA drug label records list LIDOCAINE, MENTHOL as the active ingredient. Products with the same active ingredient can usually be substituted only when a prescriber or pharmacist confirms it is appropriate.

Has ZHI Technologies been recalled?
No FDA recall record in our database matches this product name or manufacturer. Recall data is updated periodically, so a very recent notice may not appear here yet.

Where does this information come from?
All content is reproduced from FDA Structured Product Labelling data via openFDA. It is provided for identification and reference only and is not medical advice.