Lidocaine Plantar Relief Roll-On
Lidocaine Plantar Relief Roll-On is an FDA drug label for the active ingredient LIDOCAINE manufactured by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. 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 20260805.
- Generic name
- LIDOCAINE
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 83602-211
- Application
- M017
- Label effective
- 20260805
About this product
Lidocaine Plantar Relief Roll-On is an FDA-registered drug product whose active ingredient is LIDOCAINE. It is labelled by Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83602-211, application M017, label effective 20260805. 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: temporarily relieves, muscle soreness, minor joint, wrist knees, back neck, hips shoulders. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.
Dosage & Administration
Directions Adult and Children above12 years old: · apply a thin layer to affected area every 6 to 8 hours, not more than 3 to 4 times daily · massage until thoroughly absorbed into skin · wash hands thoroughly with soap and water after each use · children under 12 years of age: ask a doctor
Warnings
Warnings For external use only
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View labelHow 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 form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | 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 Lidocaine Plantar Relief Roll-On used for?
Uses Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.
Who makes Lidocaine Plantar Relief Roll-On?
Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. is the labeler of record for Lidocaine Plantar Relief Roll-On. 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 Lidocaine Plantar Relief Roll-On 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 Lidocaine Plantar Relief Roll-On 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 Lidocaine Plantar Relief Roll-On 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.