MOROVAN

LIDOCAINE TOPICAL HUMAN OTC DRUG

MOROVAN is an FDA drug label for the active ingredient LIDOCAINE manufactured by HONG KONG UNORDERED TRADING CO., LIMITED administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20260625.

Generic name
LIDOCAINE
Manufacturer
HONG KONG UNORDERED TRADING CO., LIMITED
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
87800-2624
Application
M017
Label effective
20260625

About this product

MOROVAN is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by HONG KONG UNORDERED TRADING CO., LIMITED taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87800-2624, application M017, label effective 20260625. It is one of 152 FDA drug label records sharing the active ingredient LIDOCAINE. 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.

What it is used for

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

Active ingredients

Active ingredient Lidocaine 4%

Indications & Usage

Uses For the temporary relief of local pain.

Dosage & Administration

Directions Adults and children 12 years and older: Clean and dry the affected skin area, apply an appropriate amount uniformly. Use no more than 3 to 4 times daily. Children under 12 years of age: Consult a doctor before use.

Warnings

Warnings For external use only. Do not use On large areas of damaged skin, blistered skin, or open wounds. When using this product Avoid contact with eyes. If contact occurs, rinse thoroughly with copious amounts of water. Stop use and ask a doctor if Redness, swelling, or allergic reaction develops. Symptoms persist or condition worsens.

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How products containing LIDOCAINE compare

FDA lists 152 drug label records with LIDOCAINE 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.

Dosage formProductsManufacturerProducts
— — Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. 10
— — Shanghai Chuangshi Medical Technology (Group) Co., Ltd. 9
— — Proficient Rx LP 6
— — Bryant Ranch Prepack 5
— — Preferred Pharmaceuticals Inc. 5

Frequently asked questions

What is MOROVAN used for?
Uses For the temporary relief of local pain.

Who makes MOROVAN?
HONG KONG UNORDERED TRADING CO., LIMITED is the labeler of record for MOROVAN. 152 FDA label records share the active ingredient LIDOCAINE, 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 MOROVAN come in?
administered by topical. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.

Is MOROVAN 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?
Yes. 152 FDA drug label records list LIDOCAINE 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 MOROVAN 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.

This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.