Label: MENTHOL 6.5%- menthol, unspecified form patch

  • NDC Code(s): 71391-124-18, 71391-124-36
  • Packager: Unexo Life Sciences, Private Limited
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph not final

DISCLAIMER: Most OTC drugs are not reviewed and approved by FDA, however they may be marketed if they comply with applicable regulations and policies. FDA has not evaluated whether this product complies.

Drug Label Information

Updated January 18, 2022

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

  • SPL UNCLASSIFIED SECTION

    Drug Facts

  • Active Ingredient

    Menthol 6.5% - Topical Analgesic

  • Uses

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

    • Simple backache
    • Arthritis
    • Sprains
    • Strains
    • Bruises
  • Warnings

    For external use only

    Do not use

    • On wounds or damaged skin
    • With a heating pad

    Ask a doctor before use if you have

    • Redness over affected area

    When using this product

    • Avoid contact with eyes and mucous membranes
    • Do not bandage tightly

    Stop use and ask a doctor if

    • Condition worsens or if symptoms persist for more than 7 days or clear up and occur again within a few days
    • Excessive skin irritation occurs

    Keep out of reach of children. If swallowed, get medical help or contact a Poison Control Center right away.

  • Directions

    • Adults and children 12 years of age and older apply to the affected area no more than 3 to 4 times daily
    • Open pouch & remove patch
    • Peel off protective film and apply sticky side to affected area
    • Children under 12 years of age consult a doctor
  • Other Information

    • Store at room temperature below 80°F (27°C)
  • Inactive Ingredients

    carboxymethylcellulose sodium, camphor, DMDM hydantoin, dihydroxyl aluminium aminoacetate, emulsifying wax, edetate disodium, glycerin, polysorbate 20, polyvinyl alcohol, polyvinylpyrrolidone, sodium polyacrylate, tartaric acid, titanium dioxide, water

  • Questions

    Call +91 9212228401

  • SPL UNCLASSIFIED SECTION

    Manufactured By:
    UNEXO LIFE SCIENCES PVT. LTD.
    B-16. Sector 4, Bawana Industrial Area,
    Delhi – 110039 (INDIA)

  • PRINCIPAL DISPLAY PANEL - 1 Patch Pouch

    Lasts Up to 8 Hours!

    MENTHOL 6.5%
    PATCH

    ULTRA
    STRENGTH

    Pain Relief
    PATCH
    6.5%
    Menthol

    For Shoulders, Arms,
    Neck and Legs

    Relieves Sore Muscles & Arthritis Pain

    • Deep Penetrating. No Mess
    • Comfortable, Breathable & Stays on Securely

    1 Large Medicated Patch 5 ½ x 4 in (14 x 10 cm)

    PRINCIPAL DISPLAY PANEL - 1 Patch Pouch
  • INGREDIENTS AND APPEARANCE
    MENTHOL 6.5% 
    menthol, unspecified form patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:71391-124
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    menthol, unspecified form (UNII: L7T10EIP3A) (menthol, unspecified form - UNII:L7T10EIP3A) menthol, unspecified form910 mg
    Inactive Ingredients
    Ingredient NameStrength
    CARBOXYMETHYLCELLULOSE (UNII: 05JZI7B19X)  
    CAMPHOR (SYNTHETIC) (UNII: 5TJD82A1ET)  
    DMDM hydantoin (UNII: BYR0546TOW)  
    DIHYDROXYALUMINUM AMINOACETATE (UNII: DO250MG0W6)  
    WHITE WAX (UNII: 7G1J5DA97F)  
    Edetate Sodium (UNII: MP1J8420LU)  
    Glycerin (UNII: PDC6A3C0OX)  
    Polysorbate 20 (UNII: 7T1F30V5YH)  
    Polyvinyl Alcohol, Unspecified (UNII: 532B59J990)  
    POVIDONE K60 (UNII: SZR7Z3Q2YH)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    Tartaric acid (UNII: W4888I119H)  
    Titanium dioxide (UNII: 15FIX9V2JP)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:71391-124-1818 in 1 BOX04/01/2020
    11 in 1 POUCH; Type 0: Not a Combination Product
    2NDC:71391-124-3636 in 1 BOX04/01/2020
    21 in 1 POUCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34804/01/2020
    Labeler - Unexo Life Sciences, Private Limited (872260479)
    Establishment
    NameAddressID/FEIBusiness Operations
    Unexo Life Sciences, Private Limited872260479MANUFACTURE(71391-124)