EAYONYUMT NECK PAIN RELIEF

EAYONYUMT NECK PAIN RELIEF is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Wuhan Ruihengjie Technology Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87721-004, application M017, label effective 20260830. It is one of 193 FDA drug label records sharing the active ingredient 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 MENTHOL are most often described in connection with: affected area, directions adults, children years, older clean, remove protective, apply patch, times daily. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Directions Adults and children 12 years and older clean and dry the affected area remove protective film and apply 1 patch to the affected area remove after no more than 8 hours use up to 3 times daily

remove protective film and apply 1 patch to the affected area remove after no more than 8 hours use up to 3 times daily

Warnings For external use only. Do not use on wounds or damnaged skin with a heating pad on inritated or infected skin When using this product use only as directed avoid contact with eyes and mucous membrares do not bandage lightly Stop use and ask a doctor if conditions worsens symptoms clear up and occur again within a tew days symptoms persist far more than 7 days excessive irritation develops If pregnant or breast-leeding, ask a health professional before use

FDA lists 193 drug label records with 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 EAYONYUMT NECK PAIN RELIEF used for?
Directions Adults and children 12 years and older clean and dry the affected area remove protective film and apply 1 patch to the affected area remove after no more than 8 hours use up to 3 times daily

Who makes EAYONYUMT NECK PAIN RELIEF?
Wuhan Ruihengjie Technology Co., Ltd. is the labeler of record for EAYONYUMT NECK PAIN RELIEF. 193 FDA label records share the active ingredient 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 EAYONYUMT NECK PAIN RELIEF 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 EAYONYUMT NECK PAIN RELIEF 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 MENTHOL?
Yes. 193 FDA drug label records list 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 EAYONYUMT NECK PAIN RELIEF 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.