4Jointz

MENTHOL TOPICAL HUMAN OTC DRUG

4Jointz is an FDA drug label for the active ingredient MENTHOL manufactured by ARP(USA) Pty Ltd 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 20260413.

Generic name
MENTHOL
Manufacturer
ARP(USA) Pty Ltd
Product type
HUMAN OTC DRUG
Route
TOPICAL
Dosage form
N/A
NDC
71282-022
Application
M017
Label effective
20260413

About this product

4Jointz is an FDA-registered drug product whose active ingredient is MENTHOL. It is labelled by ARP(USA) Pty Ltd taken by topical and marketed as a human otc drug product. Identifiers on file: NDC 71282-022, application M017, label effective 20260413. 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: temporarily relieves, pains muscles, joints associated, arthritis simple, backache 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 Menthol 1.5%

Indications & Usage

Uses Temporarily relieves the aches and pains of muscles and joints associated with: ■ arthritis ■ simple backache ■ strains ■ bruises ■ sprains

Dosage & Administration

Directions: Shake well and use only as directed ■ Adults & children 12 years & older. For optimal results massage gently 3 times daily until fully absorbed.

Warnings

Warnings For external use only.

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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 4Jointz used for?
Uses Temporarily relieves the aches and pains of muscles and joints associated with: ■ arthritis ■ simple backache ■ strains ■ bruises ■ sprains

Who makes 4Jointz?
ARP(USA) Pty Ltd is the labeler of record for 4Jointz. 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 4Jointz 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 4Jointz 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 4Jointz 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.