FDA.reportPublic FDA data

4Jointz

Manufacturer
ARP(USA) Pty Ltd
Effective date
2024-12-28
Label type
HUMAN OTC DRUG LABEL
Version
10
Source
legacy-cache
Hydrated at
2026-08-01 20:44:03

Label at a glance#

Product4Jointz
Active ingredientMENTHOL
Label structure13 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

■ on open wounds or abraded skin or while nursing

■ on a child under 12 years of age with arthritis-like conditions

■ near the eyes or on mucous membranes

■ with a heating pad or bandage tightly over the area

OTC - ASK DOCTOR SECTION

Discontinue use and consult a doctor if

■ conditions worsen or symptoms persists for more than

  7 days or clear up and occur again within a few days

■ 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 Use only as directed

■ adults & children 12 years and older: massage gently

into affected joints

■ apply three (3) times daily for optimal results

OTHER SAFETY INFORMATION

Other Information store below 30°C (86°F)

Inactive Ingredients

INACTIVE INGREDIENT SECTION

Inactive ingredients Aloe barbadensis leaf gel,

caprylyl glycol, castor oil, cetyl alcohol, deionized

water, dimethicone, disiloxane,eucalypyus oil,

frankincense oil, glycerin, glyceryl stearate, olive oil,

PEG-100 stearate, phenoxyethanol, propylene glycol,

SD alcohol, sodium hydroxide, sorbic acid, symphytum

officinale (comfrey), tannic acid, urea, xanthan gum  

Questions

OTC - QUESTIONS SECTION

1-844-4JOINTZ (1-844-456-4689)

4JOINTZ®

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

Principal Display Panel

Live Pain Free

4JOINTZ®
FREEDOM TO MOVE

Pain Relief Cream

www.4jointz.com

 2 X 3.5 oz [100g] tubes – 7 oz [200g] total

Clinically Tested Long Lasting Results

4JOINTZ®
FREEDOM TO MOVE

Uniquely Formulated for Painful, Stiff & Swollen Joints

4JOINTZ®
FREEDOM TO MOVE

Nature & Science Combined
4JOINTZ®
FREEDOM TO MOVE

Nature & Science Combined

0  80119 61913  3

Manufactured for ARP (USA) Pty Ltd, 2A, Ground Floor, 15 Lake St.

Varsity Lakes QLD 4227 Australia. Visit www.4Jointz.com for further

details and to see how 4Jointz has helped people just like you.

Net wt. 7oz (200g). Patent: www.4jointz.com/patent

Made in the USA of US and imported materials

4Jointz Box V54Jointz Box V5

↓Inner Package↓

4Jointz Tube V54Jointz Tube V5

res

FDA-Initiated Inactive NDC Indexing#

NDC, Effective, Action table
NDCEffectiveActionDocumentIndexing SPLRelated label
71282-011-272021-09-07C16284748780-1ba0f9c33-4d33-a910-e053-dadaa90a0b854Jointz ®
71282-011-272021-01-29C16284748780-1ba0f9c33-4d33-a910-e053-dadaa90a0b854Jointz ®

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
71282-0114JOINTZ (MENTHOL) CREAM [ARP(USA) PTY LTD]10Legacy NDC20241229_37437b26-17ae-47f4-a23a-6fda95d3aa0b.zip

Products#

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

DailyMed product names page 1 of 1 · 24 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
71282-01171282-011-27

Ingredients#

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

DailyMed ingredient rows page 1 of 1 · 23 matching rows.

Name, UNII, Kind table
NameUNIIKind
MENTHOLL7T10EIP3AACTIB
ALOE VERA LEAFZY81Z83H0XIACT
CAPRYLYL GLYCOL00YIU5438UIACT
CASTOR OILD5340Y2I9GIACT
CETYL ALCOHOL936JST6JCNIACT
DIMETHICONE92RU3N3Y1OIACT
HEXAMETHYLDISILOXANED7M4659BPUIACT
EUCALYPTUS OIL2R04ONI662IACT
FRANKINCENSE OIL67ZYA5T02KIACT
GLYCERINPDC6A3C0OXIACT
GLYCERYL MONOSTEARATE230OU9XXE4IACT
OLIVE OIL6UYK2W1W1EIACT
PEG-100 STEARATEYD01N1999RIACT
PHENOXYETHANOLHIE492ZZ3TIACT
PROPYLENE GLYCOL6DC9Q167V3IACT
ALCOHOL3K9958V90MIACT
SODIUM HYDROXIDE55X04QC32IIACT
SORBIC ACIDX045WJ989BIACT
SYMPHYTUM OFFICINALE WHOLEH8FJJ6KX5YIACT
TANNIC ACID28F9E0DJY6IACT
UREA8W8T17847WIACT
WATER059QF0KO0RIACT
XANTHAN GUMTTV12P4NEEIACT

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
7d8545bb-29d0-48f2-bec1-a14b9da6f2dc37437b26-17ae-47f4-a23a-6fda95d3aa0b2026-04-10WarningsExact identifier
spl set id: 37437b26-17ae-47f4-a23a-6fda95d3aa0b

Reported adverse events (FAERS/openFDA)#

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