ZIMS MAX FREEZE LEG CRAMP

MENTHOL TOPICAL HUMAN OTC DRUG

ZIMS MAX FREEZE LEG CRAMP is an FDA drug label for the active ingredient MENTHOL manufactured by KOBAYASHI Healthcare International, 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 20231116.

Generic name
MENTHOL
Manufacturer
KOBAYASHI Healthcare International, Inc.
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
54273-011
Application
M017
Label effective
20231116

About this product

ZIMS MAX FREEZE LEG CRAMP is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by KOBAYASHI Healthcare International, Inc. taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 54273-011, application M017, label effective 20231116. 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, pains muscles, joints associated, simple backache, arthritis strains, bruises sprains. Wording differs between labels, and the full indications section on this page takes precedence when it is present.

Active ingredients

Active ingredients Purpose Camphor 3.1% Topical analgesic Menthol 5% Topical analgesic Methyl Salicylate 11.5% Topical analgesic

Indications & Usage

Uses For the temporary relief of minor aches and pains of muscles and joints associated with: Simple backache Arthritis Strains Bruises Sprains Cramps

Dosage & Administration

Directions Adults and children 12 years of age and over: apply to affected area not more than 4 times daily Children under 12 years of age: consult a doctor

Warnings

Warnings For external use only Flammable Keep away from fire or flame and heated surfaces Do not use if you are allergic to any ingredient in this product on open wounds, damaged or irritated skin after expiration date When using this product to avoid excess application, press applicator gently against skin do not bandage tightly or cover with wrap or use heating pad or TENS device do not use 1 hour prior to bathing or within 30 minutes after bathing do not use other than as directed avoid contact with eyes or mucous membranes Stop use and ask a doctor if condition worsens rash, itching, redness, or excessive irritation, burning sensation, swelling or blistering of the skin develops symptoms persist for more than 7 days symptoms clear up and occur again within a few days If you are pregnant or breastfeeding, ask a health professional before use. Keep out of reach of children and pets. If swallowed, get medical help, or contact a Poison Control Center immediately.

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How 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 formProductsManufacturerProducts
— — 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 ZIMS MAX FREEZE LEG CRAMP used for?
Uses For the temporary relief of minor aches and pains of muscles and joints associated with: Simple backache Arthritis Strains Bruises Sprains Cramps

Who makes ZIMS MAX FREEZE LEG CRAMP?
KOBAYASHI Healthcare International, Inc. is the labeler of record for ZIMS MAX FREEZE LEG CRAMP. 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 ZIMS MAX FREEZE LEG CRAMP 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 ZIMS MAX FREEZE LEG CRAMP 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 ZIMS MAX FREEZE LEG CRAMP 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.