BLUE SPRING Foot and Leg Comfort

BLUE SPRING Foot and Leg Comfort is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by ACA MANAGEMENT LLC taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 83591-418, 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.

Across FDA labelling, products containing MENTHOL are most often described in connection with: temporary relief, minor aches, pains muscles. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Uses: Temporary relief of minor aches and pains of muscles and joints.

Directions: For adults and children 2 years of age and older: apply to affected area not more than 3 or 4 times a day. Consult a doctor before using for children under 2 years of age.

Warnings: For external use only. Do not use on wounded, damaged or irritated skin. When using this product avoid contact with eyes or mucous membranes, do not bandage tightly. Stop use and ask a doctor if you experience a rash and/or a reaction, condition worsens, or if symptoms persist for more than 10 days or clear up and occur again within a few days. If pregnant or Breast-Feeding ask a health professional before use. Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

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.

What is BLUE SPRING Foot and Leg Comfort used for?
Uses: Temporary relief of minor aches and pains of muscles and joints.

Who makes BLUE SPRING Foot and Leg Comfort?
ACA MANAGEMENT LLC is the labeler of record for BLUE SPRING Foot and Leg Comfort. 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 BLUE SPRING Foot and Leg Comfort 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 BLUE SPRING Foot and Leg Comfort 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 BLUE SPRING Foot and Leg Comfort 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.