4Jointz

Manufacturer
ARP(USA) Pty Ltd
Effective date
2026-04-13
Label type
HUMAN OTC DRUG LABEL
Version
1
Source
full-release
Hydrated at
2026-06-01 01:53:35

Label at a glance#

Product4Jointz
Active ingredientMENTHOL
Label structure12 sections

Label contents#

Full prescribing information#

SPL UNCLASSIFIED SECTION

Drug Facts

OTC - ACTIVE INGREDIENT SECTION

Active ingredients

Menthol 1.5%

OTC - PURPOSE SECTION

Purpose

Topical analgesic

INDICATIONS & USAGE SECTION

Uses Temporarily relieves the aches and pains of muscles and joints associated with:

■ arthritis ■ simple backache  ■ strains ■ bruises ■ sprains

WARNINGS SECTION

Warnings For external use only.

OTC - DO NOT USE SECTION

Do not use
■ With warming or cooling pads/devices
■ on open wounds or damaged skin or near the eyes
■ on a child under 12 years of age with arthritis-like symptoms

OTC - ASK DOCTOR SECTION

Ask a doctor if
■ condition worsens
■ redness or irritation develops

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of the reach of children. If swallowed,

get medical help or contact a Poison Control Center right away.

DOSAGE & ADMINISTRATION SECTION

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

OTHER SAFETY INFORMATION

Store below 30°C (86°F) Do not expose to direct sunlight
or extreme heat as that can cause the natural oils to
separate which is easily resolved with shaking the tube
well.

INACTIVE INGREDIENT SECTION

Inactive ingredients: Purified Water, Aloe Barbadensis
Juice, Urea, Cetyl Alcohol, Denatured Alcohol, Glyceryl Stearate,
Olive Oil, Propylene Glycol, Symphytum Officinale (Comfrey) Extract,
Tannie Acid, PEG 100 Stea rate, Glycerin USP, Trisiloxane, Castor Oil,
Boswellia Carterii (Frankincense) Oil, Xantham Gum, Dimethicone,
Phenoxyethanol (and) Caprylyl Glycol (and) Sorbic Acid,
Sodium Hydroxide

              4JOINTZ® Package Labeling​

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

------------------------------------------------------------------

Live Pain Free

4JOINTZ®
FREEDOM TO MOVE

Live Pain Free

www.4jointz.com

2x3.5 oz (100g) tubes - 7oz (200g) total

Pain Relief Cream

Manufactured for ARP (USA) Pty Ltd, Level 2, Corporate Centre
One, 2 Corporate Court, Bunda II, Queensland 4217, Australia.
For more information visit www.4jointz.com and see how
4Jointz has helped people restore their confidence with
their freedom to move.
Proudly made in the USA.

image descriptionimage description

Tube Label 4Jointz -22Tube Label 4Jointz -22

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DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
1045482menthol 1.5 % Topical CreamPSN1
1045482menthol 15 MG/ML Topical CreamSCD1
1045482menthol 1.5 % Topical CreamSY1

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
ebc62596-fc97-4d03-9483-7ba095d25db7Product name120151210

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
71282-022-274Jointz2 in 1 PACKAGECREAM21
71282-022-274Jointz100 g in 1 TUBECREAM1001

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 23 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71282-02271282-022-27

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 22 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
4JointzMENTHOLARP(USA) Pty Ltd94a5b5f5-abf7-40b3-9dd7-43e2c22f138e2026-04-13WarningsExact identifier
ndc (package): 71282-022-27
ndc (product): 71282-022
ndc11 (package): 71282002227
spl id: f1e938da-1eef-4f90-aaf3-7a9e13126c5b
spl set id: 94a5b5f5-abf7-40b3-9dd7-43e2c22f138e

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.