XPECT STOPAIN CLINICAL- menthol spray

Xpect Stopain Clinical by

Drug Labeling and Warnings

Xpect Stopain Clinical by is a Otc medication manufactured, distributed, or labeled by Cintas Corporation. Drug facts, warnings, and ingredients follow.

Drug Details [pdf]

Active ingredient

Menthol 10.0%

Purpose

Topical Analgesic

Uses

For the temporary relief of minor aches and pains of muscles and joints associated with:

• simple backache
• arthritis
• strains
• bruises
• sprains

Warnings

For external use only. Avoid contact with eyes.

Flammable: Keep away from fire or flame.

Contents under pressure: do not puncture or incinerate. Do not store at temperature above 120°F.

WHEN USING

When using the product

• use only as directed
• do not bandage tightly or use a heating pad
• do not apply to wounds or damaged skin

STOP USE

Stop use and ask a doctor if

• condition worsens, or if symptoms persist for more than 7 days or clear up and occur again within a few days
• redness is present
• excessive irritation of the skin develops

PREGNANCY OR BREAST FEEDING

If pregnant or breast-feeding, ask a health professional before use. 

KEEP OUT OF REACH OF CHILDREN

Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away. 

Directions

Adults and children 2 years of age and older:

• apply directly onto affected area, not more than 3 to 4 times daily
• wash hands after use

Children under 2 years of age: do not use, consult a doctor

Other information

• Store at room temperature

Inactive ingredients

boswellia serrata extract, dimethylsulfone (MSM), eucalyptus oil, glucosamine sulfate, glycerin, PEG-8 dimethicone, pentylene glycol, peppermint oil, SD alcohol 39C, water (USP). 

Questions or comments?

1-877-973-2811

SPL UNCLASSIFIED SECTION

Principal Dispay 42961-257-01

Xpect Stopain Clinical Spray Label

INGREDIENTS AND APPEARANCE

XPECT STOPAIN CLINICAL 
menthol spray

Product Information
Product Type	HUMAN OTC DRUG	Item Code (Source)	NDC: 42961-257
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
BOSWELLIA SERRATA OIL (UNII: 5T1XCE6K8K)
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)
EUCALYPTUS OIL (UNII: 2R04ONI662)
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)
GLYCERIN 1,2-DIMETHYL ETHER (UNII: 21JG3RIJ74)
PEG-8 DIMETHICONE (UNII: GIA7T764OD)
PENTYLENE GLYCOL (UNII: 50C1307PZG)
PEPPERMINT OIL (UNII: AV092KU4JH)
ALCOHOL (UNII: 3K9958V90M)
WATER (UNII: 059QF0KO0R)

Packaging
#	Item Code	Package Description	Marketing Start Date	Marketing End Date
1	NDC: 42961-257-01	88 mL in 1 CAN; Type 0: Not a Combination Product	05/13/2025

Marketing Information
Marketing Category	Application Number or Monograph Citation	Marketing Start Date	Marketing End Date
OTC Monograph Drug	M017	05/13/2025

Labeler - Cintas Corporation (056481716)