Label: 4JOINTZ- menthol cream
- NDC Code(s): 71282-022-27
- Packager: ARP(USA) Pty Ltd
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated April 13, 2026
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- SPL UNCLASSIFIED SECTION
- ACTIVE INGREDIENT
- PURPOSE
- INDICATIONS & USAGE
- WARNINGS
- DO NOT USE
- ASK DOCTOR
- KEEP OUT OF REACH OF CHILDREN
- DOSAGE & ADMINISTRATION
- OTHER SAFETY INFORMATION
-
INACTIVE INGREDIENT
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
------------------------------------------------------------------
Live Pain Free
4JOINTZ®
FREEDOM TO MOVELive 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.

res
-
INGREDIENTS AND APPEARANCE
4JOINTZ
menthol creamProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:71282-022 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 1.5 g in 100 g Inactive Ingredients Ingredient Name Strength WATER (UNII: 059QF0KO0R) ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB) UREA (UNII: 8W8T17847W) CETYL ALCOHOL (UNII: 936JST6JCN) ALCOHOL (UNII: 3K9958V90M) GLYCERYL STEARATE (UNII: 230OU9XXE4) OLIVE OIL (UNII: 6UYK2W1W1E) PROPYLENE GLYCOL (UNII: 6DC9Q167V3) SYMPHYTUM OFFICINALE WHOLE (UNII: H8FJJ6KX5Y) TANNIC ACID (UNII: 28F9E0DJY6) PEG-100 MONOSTEARATE (UNII: YD01N1999R) GLYCERIN (UNII: PDC6A3C0OX) TRISILOXANE (UNII: 9G1ZW13R0G) CASTOR OIL (UNII: D5340Y2I9G) FRANKINCENSE OIL (UNII: 67ZYA5T02K) XANTHAN GUM (UNII: TTV12P4NEE) DIMETHICONE (UNII: 92RU3N3Y1O) PHENOXYETHANOL (UNII: HIE492ZZ3T) CAPRYLYL GLYCOL (UNII: 00YIU5438U) SORBIC ACID (UNII: X045WJ989B) SODIUM HYDROXIDE (UNII: 55X04QC32I) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:71282-022-27 2 in 1 PACKAGE 04/01/2026 1 100 g in 1 TUBE; Type 0: Not a Combination Product Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 04/01/2026 Labeler - ARP(USA) Pty Ltd (744244375)
