Point Relief Cold Spot Pain Relieving

Point Relief Cold Spot Pain Relieving is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by Fabrication Enterprises taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 51452-036, application M017, label effective 20231105. 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: temporary relief, minor aches, joints associated, simple backache, arthritis bruises. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses: For temporary relief of minor aches and pains of the muscles and joints associated with simple backache, arthritis, bruises, strains, and/ or sprains.

Directions: Apply directly to affected area. Do not use more than four fimes per day.

Warnings: For external use only Avoid contact with eyes Do not apply to open wounds or damaged skin If symptoms persist for more than sevan days, discontinue use and consult physician Keep out of reach of children If swallowed, consult physician Do not bandage tightly

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 Point Relief Cold Spot Pain Relieving used for?
Uses: For temporary relief of minor aches and pains of the muscles and joints associated with simple backache, arthritis, bruises, strains, and/ or sprains.

Who makes Point Relief Cold Spot Pain Relieving?
Fabrication Enterprises is the labeler of record for Point Relief Cold Spot Pain Relieving. 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 Point Relief Cold Spot Pain Relieving 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 Point Relief Cold Spot Pain Relieving 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 Point Relief Cold Spot Pain Relieving 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.