Label: MEDISTIK DUAL HOT AND COLD- methyl salicylate, menthol spray
- NDC Code(s): 50231-511-11
- Packager: Natureteq Inc.
- Category: HUMAN OTC DRUG LABEL
- DEA Schedule: None
Drug Label Information
Updated January 29, 2024
If you are a consumer or patient please visit this version.
- Download DRUG LABEL INFO: PDF XML
- Official Label (Printer Friendly)
- ACTIVE INGREDIENTS
- PURPOSE
- USES
-
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
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
-
INGREDIENTS AND APPEARANCE
MEDISTIK DUAL HOT AND COLD
methyl salicylate, menthol sprayProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50231-511 Route of Administration TOPICAL Active Ingredient/Active Moiety Ingredient Name Basis of Strength Strength MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL 10 g in 100 mL METHYL SALICYLATE (UNII: LAV5U5022Y) (SALICYLIC ACID - UNII:O414PZ4LPZ) METHYL SALICYLATE 12 g in 100 mL Inactive Ingredients Ingredient Name Strength 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 Code Package Description Marketing Start Date Marketing End Date 1 NDC:50231-511-11 118 mL in 1 BOTTLE; Type 0: Not a Combination Product 02/19/2016 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/19/2016 Labeler - Natureteq Inc. (243737371)