Label: MENTHOL OVERNIGHT PAIN RELIEF GEL-PATCH- menthol patch

  • NDC Code(s): 83602-123-01, 83602-123-15
  • Packager: Guangzhou Liuquanmiao Import & Export Trade Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated February 5, 2024

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

  • Active ingredient

    Menthol 4% ...... Purpose: Topical analgesic

  • Purpose

    Topical Analgesic

  • Uses

    Temporarily relieves muscle soreness and minor joint pains in the wrist, knees, back, neck, hips, shoulders, elbows.

  • Warnings

    For external use only

  • Do not use

    ■ on wounds or damaged skin

    ■ with a heating pad or device

    ■ with other ointments, creams, sprays, or liniments

    ■ if you are allergic to any ingredients of this product

  • When using this product

    ■ use only as directed

    ■ avoid contact with the eyes, mucous membranes or rashes

    ■ do not bandage tightly

  • Stop use and ask a doctor if

    ■ skin reactions such as redness, swelling, blistering or other discomfort occur

    ■ symptoms persist for more than 7 days

  • If pregnant or breast-feeding,

    ask a health professional before use.

  • KEEP OUT OF REACH OF CHILDREN.

    If swallowed accidentally, get medical help or contact with Poison Control Center immediately.

  • Directions

    Adult and Children above 12 years old:

    ■ Clean and dry the affected area.

    ■ Tear off the protective film and apply the exposed part of the patch to the affected area.

    ■ Carefully remove remaining film while pressing the patch firmly on the skin.

    ■ Remove patch from the skin after at most 8-hour application.

    Children under age of 12: Consult a doctor

  • Inactive ingredients

    Benzalkonium Chloride, Carboxymethylcellulose Sodium, Dihydroxyaluminum Aminoacetate, Edetate Disodium, Glycerin, Kaolin, Lauralkonium Chloride, Lavender Essential Oil, L-Tartaric Acid, Mineral Oil, Petrolatum, Polyacrylic Acid, Polysorbate 80, Propylene Glycol, PVP, Sodium Polyacrylate, Titanium Dioxide, Water

  • Questions or Comments:

    sumifunofficial@gmail.com

  • Package label. Principal display panel

    0115

  • INGREDIENTS AND APPEARANCE
    MENTHOL OVERNIGHT PAIN RELIEF GEL-PATCH 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83602-123
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.04 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7)  
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311)  
    WATER (UNII: 059QF0KO0R)  
    LAURALKONIUM CHLORIDE (UNII: 07HUP5A29X)  
    LAVENDER OIL (UNII: ZBP1YXW0H8)  
    KAOLIN (UNII: 24H4NWX5CO)  
    TARTARIC ACID (UNII: W4888I119H)  
    DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K)  
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3)  
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W)  
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J)  
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP)  
    MINERAL OIL (UNII: T5L8T28FGP)  
    POLYSORBATE 80 (UNII: 6OZP39ZG8H)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    POVIDONE K90 (UNII: RDH86HJV5Z)  
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83602-123-1515 in 1 BOX02/05/2024
    1NDC:83602-123-015.5 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01702/05/2024
    Labeler - Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (418399704)
    Registrant - Guangzhou Liuquanmiao Import & Export Trade Co., Ltd. (418399704)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shanghai Chuangshi Medical Technology (Group) Co., Ltd.546872672manufacture(83602-123) , label(83602-123)