STOPAIN CLINICAL CONTINUOUS- menthol liquid 
Troy Manufacturing, Inc.

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Stopain Clinical Continuous Spray

Drug Facts

Active Ingredient

Menthol 10.0%

Purpose

Topical Analgesic   

Uses

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

Warnings

Avoid contact with eyes. For external use only.

Keep away from fire or flame. Flammable:

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

When using this product:

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

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

If pregnant or breast-feeding,

ask a health prefessional before use.

Keep out of reach of children.

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

Directions

Adults and children over 12 years:

ask a doctor. Children 12 years of younger:

Other Information

Inactive Ingredients

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

Package Labeling:

Updated Label

STOPAIN CLINICAL CONTINUOUS 
menthol liquid
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:63936-9504
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL100 mg  in 1 mL
Inactive Ingredients
Ingredient NameStrength
INDIAN FRANKINCENSE (UNII: 4PW41QCO2M)  
DIMETHYL SULFONE (UNII: 9H4PO4Z4FT)  
EUCALYPTUS OIL (UNII: 2R04ONI662)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
GLYCERIN (UNII: PDC6A3C0OX)  
PEG-8 DIMETHICONE (UNII: GIA7T764OD)  
PENTYLENE GLYCOL (UNII: 50C1307PZG)  
PEPPERMINT OIL (UNII: AV092KU4JH)  
WATER (UNII: 059QF0KO0R)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:63936-9504-4118 mL in 1 CAN; Type 0: Not a Combination Product01/01/2020
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01701/01/2020
Labeler - Troy Manufacturing, Inc. (160075248)
Registrant - Troy Manufacturing, Inc. (160075248)
Establishment
NameAddressID/FEIBusiness Operations
Troy Manufacturing, Inc.160075248manufacture(63936-9504)

Revised: 10/2023
Document Id: 0884f72a-a1eb-5ed2-e063-6294a90ae225
Set id: 65f8d212-0f0e-4893-b6af-bd68bba46443
Version: 4
Effective Time: 20231025
 
Troy Manufacturing, Inc.