Label: MEDIRELIEF ULTRA- menthol patch

  • NDC Code(s): 73486-101-25, 73486-101-35
  • Packager: FARLA MEDICAL HEALTHCARE LTD
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 23, 2024

If you are a consumer or patient please visit this version.

View All Sections
  • Drug Facts

    Active Ingredients & Purpose

    Active ingredients (in each patch)

    Purpose

    Menthol 5%.................................................................................................................................................................

    		Topical analgesic

  • Uses

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

    • simple backache
    • arthritis
    • strains
    • sprains
  • Warnings

    FOR EXTERNAL USE ONLY. Avoid contact with the eyes.

    Do not use

    • on wounds or damaged skin
    • on a tight bandage
    • with a heating pad
    • on sensitive skin
    • if allergic to any ingredients in this product

    Stop use and ask a doctor if

    • condition worsens
    • redness is present
    • symptoms persist for more than 7 days or clear up and occur again within a few days

    If pregnant of breast-feeding

    ask a health professional before use.

    KEEP OUT OF REACH OF CHILDREN

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

  • Directions

    • adults & children 12 years of age and older: apply to affected area not more than 3 to 4 times daily
    • children under 12 years of age: consult a doctor
  • Other Information

    • store at room temperature 68-77°F (20-25°C)
    • do not store in direct sunlight or expose to excessive heat and moisture

    TAMPER EVIDENT: Do not use if pouch containing the patch is torn or broken.

  • Inactive Ingredients

    carboxymethylcellulose, dihydroxyaluminum aminoacetate, glycerin, kaolin, methylparaben, mineral oil, petrolatum, polyacrylic acid, polysorbate 80, povidone, propylene glycol, propylparaben, sodium polyacrylate, tartaric acid, titanium dioxide, water.

  • Principal Display Panel

    (Medium) Patch
    NDC 73486-101-25

    (Large) Patch
    NDC 73486-101-35

    Large Patches

    Medium Patches

  • INGREDIENTS AND APPEARANCE
    MEDIRELIEF  ULTRA
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73486-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL, UNSPECIFIED FORM (UNII: L7T10EIP3A) (MENTHOL, UNSPECIFIED FORM - UNII:L7T10EIP3A) MENTHOL, UNSPECIFIED FORM5 g
    Inactive Ingredients
    Ingredient NameStrength
    GLYCERIN (UNII: PDC6A3C0OX)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    PROPYLPARABEN (UNII: Z8IX2SC1OH)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    WATER (UNII: 059QF0KO0R)  
    DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
    POVIDONE (UNII: FZ989GH94E)  
    METHYLPARABEN (UNII: A2I8C7HI9T)  
    KAOLIN (UNII: 24H4NWX5CO)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    TARTARIC ACID (UNII: W4888I119H)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73486-101-255 in 1 CARTON05/04/2020
    11 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:73486-101-355 in 1 CARTON05/04/2020
    21 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01705/04/2020
    Labeler - FARLA MEDICAL HEALTHCARE LTD (230061759)
View All Sections

Find additional resources

(also available in the left menu)

Safety

Report Adverse Events, FDA Safety Recalls, Presence in Breast Milk

Related Resources

Medline Plus, Clinical Trials, PubMed, Biochemical Data Summary

More Info on this Drug

View Labeling Archives, RxNorm, Get Label RSS Feed, View NDC Code(s)NEW!