JOINT AND MUSCLE RELIEF TOPICAL ANALGESIC- menthol cream

Joint and Muscle Relief Topical Analgesic by

Drug Labeling and Warnings

Joint and Muscle Relief Topical Analgesic by is a Otc medication manufactured, distributed, or labeled by Smart Cookie Solutions, Pure Source, LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Drug Facts

Active Ingredients

Menthol 10.00%

Purpose

Topical Analgesic

Uses:

For the temporary relief of minor aches and pains of muscles and joints

Warnings:

For external use only

Do not use

on damaged or broken skin.

When using this product

Avoid contact with the eyes. Do not bandage tightly.

Stop use and ask a doctor if

rash or irritation develops and lasts. condition worsens, or if symptoms persist for more than 7 days or clear up and occur again with in a few days.

Keep out of reach of children.

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

If pregnant or breast-feeding,

ask a health professional before use.

Directions:

Adults and children 2 years of age and older: Apply to affected area not more than 3 to 4 times daily. Children under 2 years of age: consult a  doctor.

Other information:

Protect the product in this container from excessive heat and direct sun.

Inactive ingredients:

Aloe Barbadensis Leaf Juice,Arnica Montana Extract, Capryly lGlycol, Carbomer, Dimethyl Sulfone, Disodium EDTA, Glycerin, Glyceryl Laurate, Glyceryl Undecylenate, Ilex Paraguariensis Leaf Extract, Isopropyl Alcohol, Melaleuca Alternifolia (Tea Tree) Leaf Oil, Polysorbate 20, Pyridoxine HCI, Tocopheryl Acetate, Triethanolamine, Water (Aqua)

Questions?

1-904-439-7618

Package Labeling:

INGREDIENTS AND APPEARANCE

JOINT AND MUSCLE RELIEF TOPICAL ANALGESIC 
menthol cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87282-988
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	100 mg  in 1 mL

Inactive Ingredients
Ingredient Name	Strength
ALOE VERA LEAF (UNII: ZY81Z83H0X)
ARNICA MONTANA WHOLE (UNII: O80TY208ZW)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
CARBOMER HOMOPOLYMER, UNSPECIFIED TYPE (UNII: 0A5MM307FC)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EDETATE DISODIUM (UNII: 7FLD91C86K)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL LAURATE (UNII: Y98611C087)
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)
ISOPROPYL ALCOHOL (UNII: ND2M416302)
TEA TREE OIL (UNII: VIF565UC2G)
POLYSORBATE 20 (UNII: 7T1F30V5YH)
PYRIDOXINE HYDROCHLORIDE (UNII: 68Y4CF58BV)
.ALPHA.-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
TROLAMINE (UNII: 9O3K93S3TK)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87282-988-00	100.6 mL in 1 BOTTLE; Type 0: Not a Combination Product	12/11/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	12/11/2025

Labeler - Smart Cookie Solutions (204236611)

Registrant - Pure Source, LLC (080354456)