LidoMedix
LidoMedix is an FDA drug label for the active ingredient LIDOCAINE, MENTHOL, CAMPHOR manufactured by Absolute Therapeutics, LLC 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 20260609.
- Generic name
- LIDOCAINE, MENTHOL, CAMPHOR
- Manufacturer
- Absolute Therapeutics, LLC
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 87599-150
- Application
- M017
- Label effective
- 20260609
About this product
LidoMedix is an FDA-registered drug product whose active ingredient is LIDOCAINE, MENTHOL, CAMPHOR. It is labelled by Absolute Therapeutics, LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87599-150, application M017, label effective 20260609. 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, MENTHOL, CAMPHOR are most often described in connection with: temporary relief, minor aches, pains muscles. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Use For the temporary relief of minor aches and pains of muscles and joints
Dosage & Administration
Directions Adults and children 12 years of age and over: Clean and dry affected area. Remove patch from plastic liner and place on affected area. Use 1 patch for up to 12 hours. Place used patch on the liner when not in use. Reuse the patch up to 2 times. Wash hands after applying or removing patch. Throw away the patch by folding sticky ends together. Children under 12 years of age: consult a doctor.
Warnings
Warnings For external use only Do not use More than one patch on your body at a time On cut, irritated or swollen skin On puncture wounds Over raw surfaces or blistered areas For more than one week without consulting a doctor If you are allergic to any active or inactive ingredients If pouch is damaged or opened When using this product Use only as directed Read and follow all directions and warnings on this carton Do not allow contact with the eyes Do not use at the same time as other topical analgesics Do not bandage tightly or apply local heat to the area of use Dispose of used patch in manner that always keeps product away from children and pets. Used patches still contain the drug product that can produce serious adverse effects if a child or pet chews or ingests this patch. Stop use and consult a doctor if Condition worsens Redness is present Irritation develops Symptoms persist for more than 7 days or clear up and occur again within a few days You experience signs of skin injury, such as pain, swelling or blistering where the product was applied If pregnant or breastfeeding, consult a healthcare professional before use. Keep out of reach of children and pets. If swallowed, get medical help or contact a Poison Control Center right away.
Frequently asked questions
What is LidoMedix used for?
Use For the temporary relief of minor aches and pains of muscles and joints
Who makes LidoMedix?
Absolute Therapeutics, LLC is the labeler of record for LidoMedix.
What form does LidoMedix 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 LidoMedix 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.
Has LidoMedix 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.