MEDISTIK PROFESSIONAL ICE THERAPY

Manufacturer
Natureteq Inc.
Effective date
2024-01-29
Label type
HUMAN OTC DRUG LABEL
Version
9
Source
full-release
Hydrated at
2026-06-01 00:08:01

Label at a glance#

ProductMEDISTIK PROFESSIONAL ICE THERAPY
Active ingredientMENTHOL, CAMPHOR OIL
Label structure8 sections

Indications and uses

For the temporary relief of sore muscles and joints associated with simple backache arthritis strains sprains bruises cramps

Dosage and administration

For use on adults and children over 12 years of age and older: Apply product on affected area, not more than 4 times daily children under 12 years of age: ask a doctor

Label contents#

Full prescribing information#

ACTIVE INGREDIENTS

OTC - ACTIVE INGREDIENT SECTION

Menthol 10%

Camphor 4%

PURPOSE

OTC - PURPOSE SECTION

Topical Analgesic

USES

INDICATIONS & USAGE SECTION

For the temporary relief of sore muscles and joints associated with

  • simple backache
  • arthritis
  • strains
  • sprains
  • bruises
  • cramps

WARNINGS

WARNINGS SECTION

When using this product

  • use only as directed
  • avoid getting into the eyes and mucous membranes
  • do not bandage tightly or use with a heating pad
  • do not apply to wounds or damaged skin

Stop use and ask doctor if

  • condition worsens
  • symptoms persist for more than 7 days or clear up and occur again within a few days
  • excessive skin irritation or redness occurs

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

DIRECTIONS

DOSAGE & ADMINISTRATION SECTION

  • For use on adults and children over 12 years of age and older: Apply product on affected area, not more than 4 times daily
  • children under 12 years of age: ask a doctor

INACTIVE INGREDIENTS

INACTIVE INGREDIENT SECTION

Denatured alcohol, Water, Peppermint oil, Glycerin, Polyacrylate Crosspolymer-6, MSM, Ilex paraguariensis leaf extract, Glucosamine sulphate, Chondroitin sulphate, Folic acid, Vitamin C, Vitamin D.

OTC - KEEP OUT OF REACH OF CHILDREN SECTION

Keep out of reach of children to avoid accidental ingestion. If swallowed, get medical help or contact a Poison Control Center immediately.

PACKAGE LABEL.PRINCIPAL DISPLAY PANEL

01b LBL_NTQ_Medistik Professional Ice Therapy Roll-on01b LBL_NTQ_Medistik Professional Ice Therapy Roll-on

DailyMed RxNorm Mappings#

RxCUI, RxNorm string, TTY table
RxCUIRxNorm stringTTYSPL version
2370887camphor 4 % / menthol 10 % Topical SolutionPSN9
2370887camphor 40 MG/ML / menthol 100 MG/ML Topical SolutionSCD9
2370887camphor 4 % / menthol 10 % Topical SolutionSY9

DailyMed Product Concepts#

Product concept, Relation, Version table
Product conceptRelationVersionEffective
91c62db0-0295-c81c-d10a-0856c259edd6Product name220200428
d32bc2b8-0bb7-2216-87aa-24639646e202Product name320190619

DailyMed Package Descriptions#

Package NDC, Product, Description table
Package NDCProductDescriptionFormQuantityStrengthSPL version
50231-422-12MEDISTIK PROFESSIONAL ICE THERAPY89 mL in 1 BOTTLESOLUTION899

DailyMed Dashboard NDC Coverage#

NDC, Dashboard title, SPL version table
NDCDashboard titleSPL versionValidationDashboard ZIP
50231-422MEDISTIK PROFESSIONAL ICE THERAPY (MENTHOL, CAMPHOR) SOLUTION [NATURETEQ INC.]9Legacy NDC, 1 package rows20240130_f886e161-e84c-44d7-812c-8376e1aeabc1.zip

Products#

Every source-derived product name is available through these pages.

DailyMed product names page 1 of 1 · 16 matching rows.

NDC Codes#

Product NDC, Package NDC table
Product NDCPackage NDC
50231-42250231-422-12

Ingredients#

Every source-derived ingredient row is available through these pages.

DailyMed ingredient rows page 1 of 1 · 14 matching rows.

Source Document#

Source XML

openFDA label cross-check#

OpenFDA label data provides additional search and identifier links. DailyMed’s Structured Product Label is the canonical label on FDA.report. Matching records are deduplicated before they are shown below.

Matched openFDA labels page 1 of 1 · 1 matching rows.

Brand, Generic, Manufacturer table
BrandGenericManufacturerSPL set IDEffective dateAvailable safety fieldsJoin
101c0c11-d9a8-0c36-e063-6394a90ab15ff886e161-e84c-44d7-812c-8376e1aeabc12024-01-29WarningsExact identifier
spl id: 101c0c11-d9a8-0c36-e063-6394a90ab15f
spl set id: f886e161-e84c-44d7-812c-8376e1aeabc1

Reported adverse events (FAERS/openFDA)#

Adverse event summaries are temporarily unavailable. Other product information remains available.