Label: PAIN RELIEF PATCH- wormwood patch

  • NDC Code(s): 84171-101-01
  • Packager: Dengzhou Juhetang Medical Equipment Co., Ltd
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated March 7, 2024

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  • SPL UNCLASSIFIED SECTION

    PAIN RELIEF PATCH

  • ACTIVE INGREDIENT

    Wormwood 24%

  • PURPOSE

    Topical analgesic

  • INDICATIONS & USAGE

    For temporary relief of pain

  • WARNINGS

    For external use only

  • DO NOT USE

    more than 1 patch at a time
    with a heating pad
    on wounds or damaged skin
    if you are allergic to any ingredients of this product

  • WHEN USING

    use only as directed
    do not bandage tightly
    avoid contact with the eyes, mucous membranes or rashes

  • STOP USE

    symptoms persist for more than 7 days
    conditions worsen
    symptoms clear up and occur again within a few days
    Localized,skin,reactions,such as rash,itching,redness ,pain,swelling and blistering develop

  • KEEP OUT OF REACH OF CHILDREN

    Keep out of reach of children.lf swallowed,get medical help or contact a Poison Control Center right away.

  • DOSAGE & ADMINISTRATION

    Adults and children 12 years of age and over:
    clean and dry affected area
    apply 1 patch at a time to affected area,not more than 3 to 4 times daily
    remove film from patch and apply to the skin
    Children under 12 years of age:consult a doctor

  • STORAGE AND HANDLING

    Store in a clean,dry place outside of direct sunlight.Protect product from excessive moisture

  • INACTIVE INGREDIENT

    Safflower
    Panax Notoginseng Root
    Lycopodium Japonicum Whole
    Ligusticum Sinense Subsp.Chuanxiong Whole
    Parsnip
    Gentiana Macrophylla Whole
    Stephania Retrandra Root
    Salvia Miltiorrhiza Whole

  • PRINCIPAL DISPLAY PANEL

    label-1label2

  • INGREDIENTS AND APPEARANCE
    PAIN RELIEF PATCH 
    wormwood patch
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84171-101
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    WORMWOOD (UNII: F84709P2XV) (WORMWOOD - UNII:F84709P2XV) WORMWOOD24 g  in 100 
    Inactive Ingredients
    Ingredient NameStrength
    LYCOPODIUM JAPONICUM WHOLE (UNII: OEI21JSS1R)  
    PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)  
    GENTIANA MACROPHYLLA WHOLE (UNII: 5HGH7AO55Y)  
    STEPHANIA TETRANDRA ROOT (UNII: 48PS81XHK0)  
    SALVIA MILTIORRHIZA WHOLE (UNII: 714783Y9Z0)  
    PARSNIP (UNII: L2V28YP49S)  
    SAFFLOWER (UNII: 4VBL71TY4Y)  
    LIGUSTICUM SINENSE SUBSP. CHUANXIONG WHOLE (UNII: CAX256379F)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84171-101-0112 in 1 PATCH; Type 0: Not a Combination Product03/07/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01703/07/2024
    Labeler - Dengzhou Juhetang Medical Equipment Co., Ltd (407101751)
    Establishment
    NameAddressID/FEIBusiness Operations
    Dengzhou Juhetang Medical Equipment Co., Ltd407101751manufacture(84171-101)
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