EASMENT DMSO CREAM- menthol 1.00% cream

Easment DMSO cream by

Drug Labeling and Warnings

Easment DMSO cream by is a Otc medication manufactured, distributed, or labeled by Easment LLC. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

ACTIVE INGREDIENT

Menthol 1.00%

PURPOSE

Topical Analgesic

DOSAGE & ADMINISTRATION

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

WARNINGS

For external use only.

• on wounds or damaged skin
• with a heating pad
• if allergic to ingredient in the product

• Avoidcontact with the eyes
• Do not bandage tightly

• rash or irritation developsand lasts
• condition worsens, or if symptoms persist for more than 7 days or clear up ad occur again within a few days

If swallowed, get medical help or contact a Poison Control Center right away. If pregnant or breast-feeding, ask a health professional before use.

INDICATIONS & USAGE

• Apply a small amount to the affected area 1-3 times daily.
• Massage gently until fully absorbed.
• Best used after warm shower or warm compress for enhanced penetration.

OTHER SAFETY INFORMATION

• Store at 20-25°C(68-77°F)
• Protect from excessive heat and direct sunlight
• Close lidtightly after use

INACTIVE INGREDIENT

WATER, DIMETHYL SULFOXIDE, ALOE BARBADENSIS LEAF JUICE, CAPRYLIC/CAPRICTRI GLYCERIDE, CETEARYL ALCOHOL DIMETHYL SULFONE, GLYCERIN, GLYCERYLSTEARATE, PEG-100 STEARATE, SODIUM ACRYLATES COPOLYMER, ARNICA MONTANA FLOWER EXTRACT, HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL, BUTYROSPERMUMPARKII (SHEA) BUTTER, MAGNESIUM CHLORIDE, METHYLENE BIS-BENZOTRIAZOLYLTETRAMETHYLBUTYLPHENOL LECITHIN, DIMETHICONE, TOCOPHERYL ACETATE,CAPRYLYL GLYCOL, ETHYLHEXYLGLYCERIN, CARBOMER, LAVANDULAANGUSTIFOLIA(LAVENDER) OIL CURCUMALONGA(TURMERIC) ROOT EXTRACT, DECYL GLUCOSIDE,ZINGIBER OFFICINALE (GINGER) ROOT EXTRACT, CAPSAICIN, AMINOMETHYLPROPANOL, SODIUM CITRATE, MENTHYL LACTATE, SORBITOL, ACRYLATES COPOLYMER

PRINCIPAL DISPLAY PANEL

INGREDIENTS AND APPEARANCE

EASMENT DMSO CREAM 
menthol 1.00% cream

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 87352-002
Route of Administration	TOPICAL

Active Ingredient/Active Moiety
Ingredient Name	Basis of Strength	Strength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A)	MENTHOL	1.15 g  in 115 g

Inactive Ingredients
Ingredient Name	Strength
PEG-100 STEARATE (UNII: YD01N1999R)
GINGER (UNII: C5529G5JPQ)
CAPRYLIC/CAPRIC TRIGLYCERIDE (UNII: C9H2L21V7U)
METHYLENE BIS-BENZOTRIAZOLYL TETRAMETHYLBUTYLPHENOL (UNII: 8NT850T0YS)
MAGNESIUM CHLORIDE (UNII: 02F3473H9O)
CAPSAICIN (UNII: S07O44R1ZM)
AMINOMETHYLPROPANOL (UNII: LU49E6626Q)
ETHYLHEXYLGLYCERIN (UNII: 147D247K3P)
SODIUM ACRYLATES CROSSPOLYMER-2 (UNII: D3HPR4WW6F)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
CURCUMA LONGA (TURMERIC) ROOT (UNII: 856YO1Z64F)
WATER (UNII: 059QF0KO0R)
CETEARYL ALCOHOL (UNII: 2DMT128M1S)
GLYCERIN (UNII: PDC6A3C0OX)
GLYCERYL STEARATE (UNII: 230OU9XXE4)
CARBOMER (UNII: 0A5MM307FC)
LAVANDULA ANGUSTIFOLIA (LAVENDER) OIL (UNII: ZBP1YXW0H8)
BUTYROSPERMUM PARKII (SHEA) BUTTER (UNII: K49155WL9Y)
LECITHIN, SOYBEAN (UNII: 1DI56QDM62)
DIMETHICONE 1000 (UNII: MCU2324216)
CAPRYLYL GLYCOL (UNII: 00YIU5438U)
GLATIRAMER ACETATE (UNII: 5M691HL4BO)
ALOE BARBADENSIS LEAF JUICE (UNII: RUE8E6T4NB)
ARNICA MONTANA FLOWER WATER (UNII: U7L2JP51PR)
HELIANTHUS ANNUUS (SUNFLOWER) SEED OIL (UNII: 3W1JG795YI)
ALPHA-TOCOPHEROL ACETATE (UNII: 9E8X80D2L0)
DECYL GLUCOSIDE (UNII: Z17H97EA6Y)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 87352-002-01	115 g in 1 CARTON; Type 0: Not a Combination Product	02/19/2026

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	02/19/2026

Labeler - Easment LLC (140938573)