Alo Therapeutic Massage
Alo Therapeutic Massage is an FDA drug label for the active ingredient MENTHOL, HISTAMINE DIHYDROCHLORIDE manufactured by CMI Therapy Solutions 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 20231110.
- Generic name
- MENTHOL, HISTAMINE DIHYDROCHLORIDE
- Manufacturer
- CMI Therapy Solutions
- Product type
- HUMAN OTC DRUG
- Route
- TOPICAL
- Dosage form
- N/A
- NDC
- 71061-763
- Application
- M017
- Label effective
- 20231110
About this product
Alo Therapeutic Massage is an FDA-registered drug product whose active ingredient is MENTHOL, HISTAMINE DIHYDROCHLORIDE. It is labelled by CMI Therapy Solutions taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71061-763, application M017, label effective 20231110. It is one of 6 FDA drug label records sharing the active ingredient MENTHOL, HISTAMINE DIHYDROCHLORIDE. 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, HISTAMINE DIHYDROCHLORIDE are most often described in connection with: temporary relief, minor aches, pains associated, backache arthritis. Wording differs between labels, and the full indications section on this page takes precedence when it is present.
Active ingredients
Indications & Usage
Uses For temporary relief of minor aches and pains associated with backache, arthritis, bruises and sprains.
Dosage & Administration
Directions Apply directly to affected area. Do not use more than four times per day.
Warnings
Warnings For external use only. Avoid contact with eyes. Do not apply to open wounds or damaged skin. 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 bandage tightly. If pregnant or breast feeding, contact physician prior to use.
More products with the same ingredient
MENTHOL, HISTAMINE DIHYDROCHLORIDEHow products containing MENTHOL, HISTAMINE DIHYDROCHLORIDE compare
FDA lists 6 drug label records with MENTHOL, HISTAMINE DIHYDROCHLORIDE 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 |
|---|---|---|---|
| — | — | CMI Therapy Solutions | 4 |
| — | — | Theraplex Solutions | 2 |
| — | — | — | — |
| — | — | — | — |
| — | — | — | — |
Frequently asked questions
What is Alo Therapeutic Massage used for?
Uses For temporary relief of minor aches and pains associated with backache, arthritis, bruises and sprains.
Who makes Alo Therapeutic Massage?
CMI Therapy Solutions is the labeler of record for Alo Therapeutic Massage. 6 FDA label records share the active ingredient MENTHOL, HISTAMINE DIHYDROCHLORIDE, 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 Alo Therapeutic Massage 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 Alo Therapeutic Massage 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, HISTAMINE DIHYDROCHLORIDE?
Yes. 6 FDA drug label records list MENTHOL, HISTAMINE DIHYDROCHLORIDE 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 Alo Therapeutic Massage 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.