Label: COLD HOT PATCH- menthol patch

  • Contains inactivated NDC Code(s)
    NDC Code(s):
    57900-002-01, 57900-002-02, 57900-002-03, 57900-002-04, view more
    57900-002-05, 57900-002-06, 57900-002-07, 57900-002-08, 57900-002-09, 57900-002-10, 57900-002-11, 57900-002-12
  • Packager: Zhejiang Bangli Medical Products CO.,LTD
  • Category: HUMAN OTC DRUG LABEL

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 March 18, 2014

If you are a healthcare professional or from the pharmaceutical industry please visit this version.

  • Active Ingredient

    Menthol 5.00%.

  • Purpose

    Topical analgesic

  • Use

    temporarily relieves minor aches and pains of muscles and joints due to
    .arthritis .simple backache .strains . sprains
    .bursitis .tendonitis . Bruises . Cramps

  • Warnning

    For external use only.
    When using this product.use only as directed . avoid contact with eyes and mucous membranes. do not apply to wounds or damaged skin.do not bandage tightly or use a heating pad
    Stop use and ask doctor if
    .excessive redness or irritation is present
    .condition worsens
    .pain persist for more than 7 days
    .symptoms clear up and occur again within a few days
    If pregnant or breast-feeding, ask a health professional before use, keep out of reach of childeren.If swallowed, get medical help or contact a poison control center right away.

    keep out of reach of childeren.If swallowed, get medical help or contact a poison control center right away.

  • Directions

    .adults and children 12 years and over: apply patch to affected area as needed but not more than 4 times daily
    .children under 12 years: ask a doctor
    . for easy application: grasp both ends of pad firmly, pull at both ends. Stretch pad until the backing separates.
    Remove protective film while applying pad directly to site of pain.

  • Inactive Ingredients

    Acrylic Acid,Aluminum Hydroxide,Carmellose Sodium,2 Ethylhexyl Acrylate,Glycerin,Isopropyl Myristate,Methyl Acrylate,Nonoxynol 30,
    Polyacrylate,Polyacrylic Acid,Polysorbate 80,Sorbitan Sesquioleate,Starch,Talc,Tartaric Acid,Titanium Dioxide,Water

  • PRINCIPAL DISPLAY PANEL

    image description

  • INGREDIENTS AND APPEARANCE
    COLD HOT PATCH 
    menthol patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:57900-002
    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
    Acrylic Acid (UNII: J94PBK7X8S)  
    Aluminum Hydroxide (UNII: 5QB0T2IUN0)  
    CROSCARMELLOSE SODIUM (UNII: M28OL1HH48)  
    2-ETHYLHEXYL ACRYLATE (UNII: HR49R9S6XG)  
    Glycerin (UNII: PDC6A3C0OX)  
    Isopropyl Myristate (UNII: 0RE8K4LNJS)  
    Methyl Acrylate (UNII: WC487PR91H)  
    NONOXYNOL-30 (UNII: JJX07DG188)  
    SODIUM POLYACRYLATE (8000 MW) (UNII: 285CYO341L)  
    POLYACRYLIC ACID (8000 MW) (UNII: 73861X4K5F)  
    Polysorbate 80 (UNII: 6OZP39ZG8H)  
    Sorbitan Sesquioleate (UNII: 0W8RRI5W5A)  
    STARCH, POTATO (UNII: 8I089SAH3T)  
    Talc (UNII: 7SEV7J4R1U)  
    Tartaric Acid (UNII: W4888I119H)  
    Titanium Dioxide (UNII: 15FIX9V2JP)  
    Water (UNII: 059QF0KO0R)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:57900-002-014 in 1 CARTON
    112 in 1 PACKAGE
    11 in 1 BOX
    12 in 1 BAG
    10.408 g in 1 PATCH
    2NDC:57900-002-023 in 1 CARTON
    212 in 1 PACKAGE
    26 in 1 BOX
    21 in 1 BAG
    20.408 g in 1 PATCH
    3NDC:57900-002-034 in 1 CARTON
    312 in 1 PACKAGE
    31 in 1 BOX
    33 in 1 BAG
    30.408 g in 1 PATCH
    4NDC:57900-002-0450 in 1 CARTON
    41 in 1 BOX
    45 in 1 BAG
    40.408 g in 1 PATCH
    5NDC:57900-002-0548 in 1 CARTON
    53 in 1 BOX
    51 in 1 BAG
    50.408 g in 1 PATCH
    6NDC:57900-002-068 in 1 CARTON
    66 in 1 PACKAGE
    61 in 1 BOX
    65 in 1 BAG
    60.408 g in 1 PATCH
    7NDC:57900-002-074 in 1 CARTON
    76 in 1 PACKAGE
    71 in 1 BOX
    75 in 1 BAG
    70.408 g in 1 PATCH
    8NDC:57900-002-084 in 1 CARTON
    850 in 1 PACKAGE
    81 in 1 BOX
    85 in 1 BAG
    80.85 g in 1 PATCH
    9NDC:57900-002-0930 in 1 CARTON
    91 in 1 BOX
    95 in 1 BAG
    90.595 g in 1 PATCH
    10NDC:57900-002-108 in 1 CARTON
    106 in 1 PACKAGE
    101 in 1 BOX
    105 in 1 BAG
    100.595 g in 1 PATCH
    11NDC:57900-002-114 in 1 CARTON
    116 in 1 PACKAGE
    111 in 1 BOX
    115 in 1 BAG
    110.595 g in 1 PATCH
    12NDC:57900-002-128 in 1 CARTON
    126 in 1 PACKAGE
    121 in 1 BOX
    123 in 1 BAG
    121.487 g in 1 PATCH
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph not finalpart34803/18/2014
    Labeler - Zhejiang Bangli Medical Products CO.,LTD (421295875)
    Establishment
    NameAddressID/FEIBusiness Operations
    Zhejiang Bangli Medical Products CO.,LTD421295875manufacture(57900-002)