Label: RELIEF- menthol patch

  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated December 11, 2023

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  • ACTIVE INGREDIENT

    Menthol (plant derived) 5%

  • PURPOSE

    Topical Analgesic

  • INDICATIONS & USAGE

  • WARNINGS

    For external use only

  • WHEN USING

    • use only as directed
    • avoid contact with the eyes and other mucous membranes
    • do not apply to wounds or damaged skin
    • do not bandage tightly
    • use only as directed
  • DO NOT USE

    • more than one patch at a time
    • at the same time as other topical analgesics
  • STOP USE

    • condition worsens
    • symptoms persist for more than 7 days or clear up and occur again within a few days
  • PREGNANCY OR BREAST FEEDING

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

  • KEEP OUT OF REACH OF CHILDREN

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

  • DOSAGE & ADMINISTRATION

    adults over 18 years:

    • use one patch
    • carefully remove the backing film and apply to the affected area no more than 3 to 4 times daily
    • each patch can be worn up to 12 hours
    • children under 18 years of age: consult a doctor
  • STORAGE AND HANDLING

    • store in a cool, dry place
  • INACTIVE INGREDIENT

    methyl acrylate, 2-ethylhexyl acrylate, acrylic acid copolymer, hydroxyethyl acrylate, vinyl acetate copolymer, lavender oil, arnica montana extract, aloe vera extract, eucalyptus oil

  • QUESTIONS

    (310) 909-8407 | thegoodpatch.com

    You may also report serious side effects to this phone number

  • PRINCIPAL DISPLAY PANEL

    Relief

    QTY. 04 PATCHES

    Pain holding you back? Keep moving with this fast-acting, water-resistant topical patch. Made with plant-derived Menthol, Lavender, Arnica, and Aloe Vera.

    Relief

  • INGREDIENTS AND APPEARANCE
    RELIEF 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:72587-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL5 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:72587-002-011 in 1 BOX04/15/2022
    11 in 1 POUCH
    11.35 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01704/15/2022
    Labeler - La Mend, Inc. (117940830)
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