24 7 Relief and Recovery Pain Relieving

24 7 Relief and Recovery Pain Relieving is an FDA-registered drug product whose active ingredient is MENTHOL, UNSPECIFIED FORM. It is labelled by Triplicare Inc taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 87656-964, application M017, label effective 20260430. It is one of 17 FDA drug label records sharing the active ingredient MENTHOL, UNSPECIFIED FORM. 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, UNSPECIFIED FORM are most often described in connection with: temporary relief, minor aches, pains sore, muscles joints, arthritis simple, backache strains, bruises sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses: Temporary relief from minor aches and pains of sore muscles & joints associated with arthritis, simple backache, strains, bruises & sprains.

Directions: Adults and children 12 years of age and older: Apply and massage on to affected areas. Repeat as needed no more than 4 times daily. Wash hands after use with cool water. Children under 12 years of age: Consult physician.

Warnings: For external use only. Use only as directed. Keep away from excessive heat or flame. When using this product: Avoid contact with the eyes or mucous membranes. Do not apply to wounds or damaged skin. Do not use with other ointments, creams, sprays or liniments. Do not apply to irritated skin or if excessive irritation develops. Do not bandage. Do not use with heating pad or device. Wash hands after use with cool water. Stop use and ask doctor if: Condition worsens, or if symptoms persist for more than 7 days, or clear up and return. If pregnant or breast-feeding: Ask a health professional before use. Keep out of the reach of children. If accidentally ingested, get medical help or contact Poison Control Center immediately.

FDA lists 17 drug label records with MENTHOL, UNSPECIFIED FORM 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 24 7 Relief and Recovery Pain Relieving used for?
Uses: Temporary relief from minor aches and pains of sore muscles & joints associated with arthritis, simple backache, strains, bruises & sprains.

Who makes 24 7 Relief and Recovery Pain Relieving?
Triplicare Inc is the labeler of record for 24 7 Relief and Recovery Pain Relieving. 17 FDA label records share the active ingredient MENTHOL, UNSPECIFIED FORM, 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 24 7 Relief and Recovery 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 24 7 Relief and Recovery 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, UNSPECIFIED FORM?
Yes. 17 FDA drug label records list MENTHOL, UNSPECIFIED FORM 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 24 7 Relief and Recovery 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.