FREEZE EASE Roll-On

FREEZE EASE Roll-On is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Global America Group LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87843-311, application M017, label effective 20260902. 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: minor aches, temporary relief, simple backache, joints associated, pains muscles, strains bruises, temporarily relieves, sore throat. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Directions adults and children 5 years of age and older: apply externally to the affected area up to 3 to 4 times daily children under 5 years of age: consult a physician wash hands after use with cool water

Warnings For external use only. Flammable: Keep away from excessive heat or open flame. When using this product use only as directed avoid contact with the theeyes or on mucous membranes do not apply to wounds or damaged skin do not apply to irritated skin or if excessive irritation develops do not bandage tightly or use with heating pad or device Stop use and ask a doctor if you experience pain, swelling or blistering of the skin condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days arthritis pain persists for more than 10 days, or rednessis present. allergic reaction occurs If pregnant or breast-feeding, ask a health professional before use. Keep out of reach of children. If swallowed, get medical help orcontact a Poison Control Center right away.

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 FREEZE EASE Roll-On used for?
The FDA label on file for this product does not include a full indications section. Other FDA labels sharing the active ingredient MENTHOL describe it in connection with: minor aches, temporary relief, simple backache, joints associated, pains muscles, strains bruises, temporarily relieves, sore throat. Check the specific product label or ask a prescriber before use.

Who makes FREEZE EASE Roll-On?
Global America Group LLC is the labeler of record for FREEZE EASE Roll-On. 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 FREEZE EASE 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 FREEZE EASE 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 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 FREEZE EASE 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.