Label: VARICOSE VEINS PATCH patch

  • NDC Code(s): 83675-001-01
  • Packager: Guangzhou Hanhai Trading Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None
  • Marketing Status: OTC monograph 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 September 13, 2023

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  • Active Ingredient

    Bormeol 12.0%

  • Purpose

    Relieve Pain

  • Use

    Varicose Veins Patch to help relieve pain on leg

  • Warnings


    For external use only.

    Keep Out Of Reach Of Children
    Pregnant, breast-feeding, people with severe chronic diseases or allergic to the raw materials are forbidden to use

  • Do not use

    Product shall not be eat

  • When Using

    Do not stick around eyes and mouth,This product cannot replace drugs.

  • Stop Use

    In case of adverse reactions, please stop using this product.If the symptoms.

  • Ask Doctor

    ask doctor in case of adverse reactions

  • Keep Oot Of Reach Of Children

    Please do not place this product where unconscious persons can reach it.

  • Directions

    After cleaning and drying the affected area, open the package to remove the back of the paper, apply 1-2 stickers at a time, apply 1-2 days for each sticker, and interval 1 day.

    Children should be used under adult supervision.

  • Other information

    Store the product in a cool, dry and well-ventilated place

    Avoid direct sunlight

  • Inactive ingredients

    Crush Chinese Angelica

    Radix Rehmanniae Recens
    Phellodendron Amurense
    Honeysuckle
    Dandelion
    Salvia Militrorrhiza
    Atractylodes Sinensis
    AstraglusBase
    Tuckahoe
    Safflower
    Licorice
    Scutellaria Baicalensis Georgi into fine powder
    Camphor
    Eucalyptus Oil

  • PRINCIPAL DISPLAY PANEL

    0102

  • INGREDIENTS AND APPEARANCE
    VARICOSE VEINS PATCH 
    varicose veins patch patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:83675-001
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    BORNEOL (UNII: M89NIB437X) (BORNEOL - UNII:M89NIB437X) BORNEOL12 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    TARAXACUM OFFICINALE (UNII: 39981FM375)  
    ATRACTYLODES LANCEA ROOT (UNII: CAZ6282J2O)  
    LICORICE (UNII: 61ZBX54883)  
    REHMANNIA GLUTINOSA ROOT (UNII: 1BEM3U6LQQ)  
    CAMPHOR (NATURAL) (UNII: N20HL7Q941)  
    FU LING (UNII: XH37TWY5O4)  
    EUCALYPTUS OIL (UNII: 2R04ONI662)  
    SAFFLOWER (UNII: 4VBL71TY4Y)  
    LONICERA CONFUSA FLOWER (UNII: 3JV904IJ0V)  
    SCUTELLARIA BAICALENSIS WHOLE (UNII: 6YF0M477I5)  
    PHELLODENDRON AMURENSE BARK (UNII: PBG27B754G)  
    ANGELICA SINENSIS ROOT (UNII: B66F4574UG)  
    SALVIA MILTIORRHIZA WHOLE (UNII: 714783Y9Z0)  
    ASTRAGALUS ALLOCHROUS WHOLE (UNII: 8849C568OC)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:83675-001-018 in 1 BAG; Type 0: Not a Combination Product09/12/2023
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC monograph finalM01609/12/2023
    Labeler - Guangzhou Hanhai Trading Co., Ltd (419707381)
    Establishment
    NameAddressID/FEIBusiness Operations
    Guangzhou Hanhai Trading Co., Ltd419707381label(83675-001) , manufacture(83675-001)
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