Nervionix Pro Magnesium Ice

Nervionix Pro Magnesium Ice is an FDA-registered drug product whose active ingredient is LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE. It is labelled by Micelle Laboratories, Incorporated taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87752-003, label effective 20260709. It is one of 3 FDA drug label records sharing the active ingredient LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE. 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 HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE are most often described in connection with: soothing relief, pain stiffness, tingling burning, arthritis muscles, joint pains, soreness backache. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses Soothing relief of pain, stiffness, tingling, or burning nerve pain associated with arthritis, muscles and joint pains, cramps and soreness, backache, and sciatica.

Directions Adults and children 12 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 12 years of age: Consult a doctor before use. We recommend testing a small amount of cream on your skin first to check for skin reaction and comfort level; wait 15 minutes before applying to affected area if you are happy with the comfort level.

Warnings For external use only. Do not use On damaged or broken skin. When using this product Avoid contact with the eyes. Do not bandage tightly. Stop use and ask a doctor if rash or irritation develops and lasts. Condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding , ask a health professional before use.

FDA lists 3 drug label records with LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE 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 Nervionix Pro Magnesium Ice used for?
Uses Soothing relief of pain, stiffness, tingling, or burning nerve pain associated with arthritis, muscles and joint pains, cramps and soreness, backache, and sciatica.

Who makes Nervionix Pro Magnesium Ice?
Micelle Laboratories, Incorporated is the labeler of record for Nervionix Pro Magnesium Ice. 3 FDA label records share the active ingredient LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE, 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 Nervionix Pro Magnesium Ice 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 Nervionix Pro Magnesium Ice 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 HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE?
Yes. 3 FDA drug label records list LIDOCAINE HYDROCHLORIDE, MENTHOL,MAGNESIUM CHLORIDE 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 Nervionix Pro Magnesium Ice 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.