Professional Therapy MuscleCare Pain Relieving Cold Gel
Professional Therapy MuscleCare Pain Relieving Cold Gel is an FDA drug label for the active ingredient CAMPHOR, MENTHOL manufactured by Active and Innovative administered by CUTANEOUS. 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 20260721.
- Generic name
- CAMPHOR, MENTHOL
- Manufacturer
- Active and Innovative
- Product type
- HUMAN OTC DRUG
- Route
- CUTANEOUS
- Dosage form
- N/A
- NDC
- 70039-285
- Application
- M017
- Label effective
- 20260721
About this product
Professional Therapy MuscleCare Pain Relieving Cold Gel is an FDA-registered drug product whose active ingredient is CAMPHOR, MENTHOL. It is labelled by Active and Innovative taken by cutaneous and marketed as a human otc drug product. Identifiers on file: NDC 70039-285, application M017, label effective 20260721. It is one of 10 FDA drug label records sharing the active ingredient CAMPHOR, 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 CAMPHOR, MENTHOL are most often described in connection with: usage indications. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Indications & Usage
Indications and Usage Indications and Usage
Dosage & Administration
Dosage And Aministration Dosage and Administration
Warnings
Warnings Warnings
More products with the same ingredient
CAMPHOR, MENTHOLEagle Brand Medicated Oil Refresh
View labelEagle Brand Medicated Roll On Refresh
View labelEagle Brand Medicated Roll On Refresh
View labelIcy Hot Pro Dry
View labelProfessional Therapy MuscleCare
View labelProfessional Therapy MuscleCare pain relieving gel Extra Strength
View labelProfessional Therapy MuscleCare pain relieving gel Extra Strength
View labelHow products containing CAMPHOR, MENTHOL compare
FDA lists 10 drug label records with CAMPHOR, 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 |
|---|---|---|---|
| — | — | Active and Innovative Inc. | 3 |
| — | — | PT. EAGLE INDO PHARMA | 2 |
| — | — | Active and Innovative | 1 |
| — | — | Borden Company (Private) Limited | 1 |
| — | — | Chattem, Inc. | 1 |
Frequently asked questions
What is Professional Therapy MuscleCare Pain Relieving Cold Gel used for?
Indications and Usage Indications and Usage
Who makes Professional Therapy MuscleCare Pain Relieving Cold Gel?
Active and Innovative is the labeler of record for Professional Therapy MuscleCare Pain Relieving Cold Gel. 10 FDA label records share the active ingredient CAMPHOR, 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 Professional Therapy MuscleCare Pain Relieving Cold Gel come in?
administered by cutaneous. Strengths and pack sizes vary by label, so compare the NDC on your pack with the identifier listed on this page.
Is Professional Therapy MuscleCare Pain Relieving Cold Gel 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, MENTHOL?
Yes. 10 FDA drug label records list CAMPHOR, 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 Professional Therapy MuscleCare Pain Relieving Cold Gel 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.