Satohap Cool and Hot Pads

Satohap Cool and Hot Pads is an FDA-registered drug product whose active ingredient is CAMPHOR, CAPSAICIN, MENTHOL. It is labelled by Sato Pharmaceutical Co., Ltd. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 49873-621, application M017, label effective 20260731. It is one of 4 FDA drug label records sharing the active ingredient CAMPHOR, CAPSAICIN, 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 CAMPHOR, CAPSAICIN, MENTHOL are most often described in connection with: temporary relief, minor aches, pains muscles, joints due, simple backache, arthritis strains, bruises sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses For the temporary relief of minor aches and pains of muscles and joints due to: simple backache arthritis strains bruises sprains

Directions Adults and children 4 years of age and older: remove polyethylene film and place adhesive pad over affected area. do not use more than 2 patches per day. Children under 4 years of age: Consult a doctor.

Warnings For external use only Do not use on irritated or damaged skin on wounds Ask a doctor or pharmacist before use if you have any concerns about using this product When using this product avoid contact with the eyes or mucus membranes do not bandage tightly do not apply heat to the area in the form of heating pads, hot water bottles, or lamps (doing so increases the risk of serious burns) Stop use and ask a doctor if condition worsens symptoms persist for more than 7 days symptoms clear up and occur again within a few days excessive irritation of the skin develops nausea, vomiting, abdominal discomfort, diarrhea, or skin rash occurs. you feel actual pain or experience blistering or burning after application (it is normal to feel a warming or cooling sensation) when using for pain or arthritis: pain persists for more than 10 days redness is present in conditions affecting children under 12 years of age Report any unexpected side effects from the use of this product to the FDA MedWatch Program Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

Report any unexpected side effects from the use of this product to the FDA MedWatch Program

FDA lists 4 drug label records with CAMPHOR, CAPSAICIN, 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 Satohap Cool and Hot Pads used for?
Uses For the temporary relief of minor aches and pains of muscles and joints due to: simple backache arthritis strains bruises sprains

Who makes Satohap Cool and Hot Pads?
Sato Pharmaceutical Co., Ltd. is the labeler of record for Satohap Cool and Hot Pads. 4 FDA label records share the active ingredient CAMPHOR, CAPSAICIN, 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 Satohap Cool and Hot Pads 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 Satohap Cool and Hot Pads 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 CAMPHOR, CAPSAICIN, MENTHOL?
Yes. 4 FDA drug label records list CAMPHOR, CAPSAICIN, 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 Satohap Cool and Hot Pads 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.