Label: ELASTIC RELIEF STRIP- menthol patch

  • NDC Code(s): 73557-130-01, 73557-130-05
  • Packager: Shanghai Chuangshi Medical Technology (Group) Co., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated April 29, 2024

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  • Active ingredient

    Menthol 5.6% ...... Purpose: Topical Analgesic

  • Purpose

    Topical Analgesic

  • Uses

    Temporary relief from minor aches and pains of sore muscles and joints associated with:

    • arthrits
    • backache
    • strains
    • sprains
  • Warnings

    • For external use only
    • Use only as directed
    • Avoid contact with eyes or mucous membranes
    • Do not apply to wounds or damaged skin
    • Do not use with other ointments, creams, sprays, or liniments
    • Do not apply to irritated skin
    • Do not overwrap or wrap strips over themselves
    • Do not bandage or use with heating pad or device
  • Ask doctor

    Stop use and ask a doctor if: You experience pain, swelling or blistering; condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

  • When using

    • Use only as directed
    • Avoid contact with eyes or mucous membranes
    • Do not apply to wounds or damaged skin
    • Do not use with other ointments, creams, sprays, or liniments
    • Do not apply to irritated skin
    • Do not overwrap or wrap strips over themselves
    • Wash hands after use with cool water
    • Do not bandage or use with heating pad or device
  • Do not use

    • Do not apply to wounds or damaged skin
    • Do not use with other ointments, creams, sprays, or liniments
    • Do not apply to irritated skin
    • Do not overwrap or wrap strips over themselves
    • Do not bandage or use with heating pad or device
  • Stop use

    Stop use and ask a doctor if: You experience pain, swelling or blistering; condition worsens, or if symptoms persist for more than 7 days, or clear up and occur again within a few days

  • Pregnancy or breast feeding

    If pregnant or breastfeeding: Ask a health professional before use

  • Keep out of reach of children

    Keep out of reach of children: If accidentally ingested, get medical help or contact a Poison Control Center immediately.

  • Directions

    • Adult and Children 12 years of age and older: Clean and dry affected area, partially peel back protective film and apply exposed strip to site of pain. Carefully remove remaining film while pressing the strip to the skin and leave in place for up to 4 hours. Do not strech the strip during application as it should be comfortable and not tight. Use on affected areas not more than 4 times daily. For best adhesion: area should be clean, dry, and smooth.
    • Children under 12 years of age: Consult physician
  • Dosage forms & strengths

    This is a strip, patch dosage form.

    The active ingredient strength is 5.6%.

  • Inactive ingredients

  • Questions

    Questions or comments: 86-21-31166566

  • Other information

    • Store in a cool dry place away from direct sunlight
  • Package label. Principal display panel

    0105

  • INGREDIENTS AND APPEARANCE
    ELASTIC RELIEF STRIP 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:73557-130
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.056 g  in 1 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYSORBATE 80 (UNII: 6OZP39ZG8H) 0.018 g  in 1 g
    GLYCERIN (UNII: PDC6A3C0OX) 0.24 g  in 1 g
    POVIDONE K90 (UNII: RDH86HJV5Z) 0.012 g  in 1 g
    GREEN TEA LEAF (UNII: W2ZU1RY8B0) 0.0001 g  in 1 g
    ALOE VERA LEAF (UNII: ZY81Z83H0X) 0.0001 g  in 1 g
    EDETATE DISODIUM (UNII: 7FLD91C86K) 0.001 g  in 1 g
    ARNICA MONTANA FLOWER (UNII: OZ0E5Y15PZ) 0.0001 g  in 1 g
    FRANKINCENSE (UNII: R9XLF1R1WM) 0.0001 g  in 1 g
    KAOLIN (UNII: 24H4NWX5CO) 0.001 g  in 1 g
    TARTARIC ACID (UNII: W4888I119H) 0.001 g  in 1 g
    WATER (UNII: 059QF0KO0R) 0.30808 g  in 1 g
    DIHYDROXYALUMINUM AMINOACETATE ANHYDROUS (UNII: 1K713C615K) 0.0015 g  in 1 g
    PROPYLENE GLYCOL (UNII: 6DC9Q167V3) 0.07 g  in 1 g
    POLYACRYLIC ACID (250000 MW) (UNII: 9G2MAD7J6W) 0.2 g  in 1 g
    CARBOXYMETHYLCELLULOSE SODIUM (UNII: K679OBS311) 0.001 g  in 1 g
    SODIUM POLYACRYLATE (2500000 MW) (UNII: 05I15JNI2J) 0.05 g  in 1 g
    TITANIUM DIOXIDE (UNII: 15FIX9V2JP) 0.001 g  in 1 g
    MINERAL OIL (UNII: T5L8T28FGP) 0.03 g  in 1 g
    PETROLATUM (UNII: 4T6H12BN9U) 0.002 g  in 1 g
    BENZALKONIUM CHLORIDE (UNII: F5UM2KM3W7) 0.001 g  in 1 g
    LAURALKONIUM CHLORIDE (UNII: 07HUP5A29X) 0.001 g  in 1 g
    NONOXYNOL-10 (UNII: K7O76887AP) 0.00002 g  in 1 g
    ISOPROPYL MYRISTATE (UNII: 0RE8K4LNJS) 0.005 g  in 1 g
    Product Characteristics
    ColorwhiteScore    
    ShapeSize
    FlavorImprint Code
    Contains    
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:73557-130-055 in 1 BOX12/30/2022
    1NDC:73557-130-019 g in 1 PATCH; Type 0: Not a Combination Product
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01712/30/2022
    Labeler - Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (546872672)
    Registrant - Shanghai Chuangshi Medical Technology (Group) Co., Ltd. (546872672)
    Establishment
    NameAddressID/FEIBusiness Operations
    Shanghai Chuangshi Medical Technology (Group) Co., Ltd.546872672manufacture(73557-130) , label(73557-130)
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