Label: MEDISTIK ICE- menthol, camphor solution
- NDC Code(s): 50231-411-11, 50231-411-12
- Packager: Natureteq Inc.
- Category: HUMAN OTC DRUG LABEL
Drug Label Information
Updated January 29, 2024
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- ACTIVE INGREDIENTS
- PURPOSE
- USES
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WARNINGS
For external use only. Avoid contact with eyes and mucous membranes. Do not apply to wounds or damaged skin. Do not tightly bandage. Do not apply with external heat, such as an electric heating pad, as this may result in excessive skin irritation or skin burn.
Stop use and consult a physician if condition worsens, rash or irritation develops, or if symptoms persist for more than 7 days or clear up and recur in a few days. Consult a health care practitioner prior to use if you are pregnant or breastfeeding. Rashes and/or burning discomfort, and hypersensitivity such as allergy have been known to occur; in which case, discontinue use.
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DIRECTIONS
For use on adults and children over 12 years of age.
Apply to affected area(s) 3 to 4 times per day as required. 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.
- INACTIVE INGREDIENTS
- KEEP OUT OF REACH OF CHILDREN
- PRINCIPAL DISPLAY PANEL
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INGREDIENTS AND APPEARANCE
MEDISTIK ICE
menthol, camphor solutionProduct Information Product Type HUMAN OTC DRUG Item Code (Source) NDC:50231-411 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 CAMPHOR OIL (UNII: 75IZZ8Y727) (CAMPHOR OIL - UNII:75IZZ8Y727) CAMPHOR OIL 4 g in 100 mL Inactive Ingredients Ingredient Name Strength ALCOHOL (UNII: 3K9958V90M) WATER (UNII: 059QF0KO0R) PEPPERMINT OIL (UNII: AV092KU4JH) GLYCERIN (UNII: PDC6A3C0OX) CARBOMER COPOLYMER TYPE A (ALLYL PENTAERYTHRITOL CROSSLINKED) (UNII: 71DD5V995L) DIMETHYL SULFONE (UNII: 9H4PO4Z4FT) ILEX PARAGUARIENSIS LEAF (UNII: 1Q953B4O4F) GLUCOSAMINE SULFATE (UNII: 1FW7WLR731) CHONDROITIN SULFATE (CHICKEN) (UNII: 7VZ9466BAB) FOLIC ACID (UNII: 935E97BOY8) ASCORBIC ACID (UNII: PQ6CK8PD0R) VITAMIN D (UNII: 9VU1KI44GP) Packaging # Item Code Package Description Marketing Start Date Marketing End Date 1 NDC:50231-411-11 89 mL in 1 BOTTLE; Type 0: Not a Combination Product 01/21/2020 2 NDC:50231-411-12 500 mL in 1 BOTTLE; Type 0: Not a Combination Product 03/18/2020 Marketing Information Marketing Category Application Number or Monograph Citation Marketing Start Date Marketing End Date OTC Monograph Drug M017 02/17/2016 Labeler - Natureteq Inc. (243737371)