MEDISTIK PROFESSIONAL DUAL ACTION- methyl salicylate, menthol spray 
Natureteq Inc.

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Natureteq (as PLD) - MEDISTICK PROFESSIONAL DUAL ACTION SPRAY (50231-521)

ACTIVE INGREDIENTS

Methyl Salicylate  12%

Menthol  10%

PURPOSE

Topical Analgesic

USES

Provides temporary soothing relief of sore muscles associated with strains and sprains, backaches, lumbago, pain of tendons
and/or ligaments as well as arthritic or rheumatic pain

WARNINGS

For external use only. Avoid contact with the eyes and mucous membranes. Do not apply to wounds or damaged skin. Do not tightly bandage. Do not inhale. Do not apply with external heat, such as an electric heating pad, as this may result in excessive skin irritation or skin burn. Keep out of the reach of children. If overdose or accidental ingestion occurs, call a Poison Control Center immediately. Consult your health care practitioner prior to use if you are pregnant or breastfeeding or if you are taking anti-coagulant medications or if you are taking medication or natural health products that cause dilation of blood vessels. Rashes and/or burning discomfort and hypersensitivity such as allergy have been known to occur; in which case; discontinue use.

DIRECTIONS

For use on adults and children over 12 years of age. For children (12 years old): Application should be supervised by an adult. Apply thinly and evenly to affected area up to 3 to 4 times per day. Rub and/or massage into skin until solution vanishes. A stinging or burning sensation will be experienced during the first few minutes as the formula begins working. For arthritis or muscle pain of the hands, retain for at least 10 minutes then wash hands. Consult your health care practitioner for use beyond 7 days

INACTIVE INGREDIENTS

Isopropyl alcohol, Water, MSM, Boswellia serrata extract, Ilex paraguariensis leaf extract, Glucosamine sulphate, Chondroitin sulphate.

KEEP OUT OF REACH OF CHILDREN

01b LBL_NTQ_Medistik Professional Dual Action Spray

MEDISTIK PROFESSIONAL DUAL ACTION 
methyl salicylate, menthol spray
Product Information
Product TypeHUMAN OTC DRUGItem Code (Source)NDC:50231-521
Route of AdministrationTOPICAL
Active Ingredient/Active Moiety
Ingredient NameBasis of StrengthStrength
MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL10 g  in 100 mL
METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE12 g  in 100 mL
Inactive Ingredients
Ingredient NameStrength
ISOPROPYL ALCOHOL (UNII: ND2M416302)  
WATER (UNII: 059QF0KO0R)  
BOSWELLIA SERRATA WHOLE (UNII: X7B7P649WQ)  
ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F)  
GLUCOSAMINE SULFATE (UNII: 1FW7WLR731)  
CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB)  
Packaging
#Item CodePackage DescriptionMarketing Start DateMarketing End Date
1NDC:50231-521-11118 mL in 1 BOTTLE; Type 0: Not a Combination Product02/19/2016
Marketing Information
Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
OTC Monograph DrugM01702/19/2016
Labeler - Natureteq Inc. (243737371)

Revised: 1/2024
Document Id: 101c14b9-b711-84bc-e063-6294a90a0f74
Set id: e0d60096-3539-49b0-adac-06bd26169ba1
Version: 10
Effective Time: 20240129
 
Natureteq Inc.