FISICO Arthrozene Pain Cream
FISICO Arthrozene Pain Cream is an FDA drug label for the active ingredient MENTHOL manufactured by FISICO INC. administered by TOPICAL. This page reproduces the FDA-approved indications and usage, dosage, contraindications, warnings, and adverse reactions exactly as published in the drug label. Data source: openFDA (U.S. FDA), label effective 20231106.
- Generic name
- MENTHOL
- Manufacturer
- FISICO INC.
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 83204-375
- Application
- M017
- Label effective
- 20231106
About this product
FISICO Arthrozene Pain Cream is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by FISICO INC. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83204-375, application M017, label effective 20231106. 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.
What it is used for
Across FDA labelling, products containing MENTHOL are most often described in connection with: temporary relief, minor aches, joints associated, arthritis simple, backache sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Indications: For the temporary relief if minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.
Dosage & Administration
Directions: Adults and children two-years of age or older: Apply to affected area not more than three to four times daily. Children under two-years of age: consult a physician.
Warnings
Warnings: For external use only When using this product avoid contact with eyes. If symptoms persist for more than seven days, discontinue use and consult physician. Keep out of reach of children. If swallowed, consult physician. Do Not Use to wounds or damaged skin. Do not bandage tightly. If pregnant or breast feeding, contact physician prior to use.
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View labelHow products containing MENTHOL compare
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.
| Dosage form | Products | Manufacturer | Products |
|---|---|---|---|
| — | — | Reckitt Benckiser LLC | 23 |
| — | — | Mondelez Global LLC | 6 |
| — | — | BLUE SPRING WELLNESS, L.L.C. | 5 |
| — | — | Shanghai Chuangshi Medical Technology (Group) Co., Ltd. | 5 |
| — | — | Bestco | 4 |
Frequently asked questions
What is FISICO Arthrozene Pain Cream used for?
Indications: For the temporary relief if minor aches and pains of the muscles and joints associated with arthritis, simple backache, sprains, bruises and strains.
Who makes FISICO Arthrozene Pain Cream?
FISICO INC. is the labeler of record for FISICO Arthrozene Pain Cream. 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 FISICO Arthrozene Pain Cream 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 FISICO Arthrozene Pain Cream 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 FISICO Arthrozene Pain Cream 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.
This page reproduces FDA Structured Product Labelling data for identification and reference. It is not medical advice, does not diagnose or treat any condition, and does not sell or price any medicine.