Label: YOUCOPIA PAIN RELIEF CREAM- pain relief cream cream

  • NDC Code(s): 82372-014-01
  • Packager: Good Manager Holdings Inc.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated November 12, 2024

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  • Active Ingredient

    Menthol 0.8%
    Camphor 0.4%

  • Purpose

    Alleviate muscle and jointpain, promoting comfortand quick recovery.

  • Use

    Suitable for sub-healthyindividuals experiencingdiscomfort caused by wind, coldand dampness, leading toblocked meridians and poorcirculation, resulting in pain anddiscomfort in the neck,shoulders, waist, knees, tendons.and heels.

  • Warnings

    For external use only.
    Do not useit on Individuals with allergies.
    Infants, children, pregnantwomen,and breastfeedingwomen should not use thisproduct.
    This product is a healthsupplement and does notreplace medications or medicaldevices for treatment.

  • Do not use

    Do Not Use on broken skin.
    Usewith caution on sensitive skin.

  • When Using

    when Using this product, keepout of eyes,ears and mouth. Incase of contact with eyes, rinseeyes thoroughly with water.

  • Stop Use

    Stop Use lf adverse reactionsoccur after use,such as rash,itching, or ulceration.

    Discontinue use and symptomswill resolve.

  • Ask Doctor

    If swallowed, get medical helpor contact a Poison ControlCenter right away.

  • Keep Oot Of Reach Of Children

    If swallowed, get medical helpor contact a Poison ControlCenter right away.

  • Directions

    For external use only.
    Clean theskin of the application area, apply this product to thedesired area, For best results,three times a day.

  • Inactive ingredients

    Chuanxiong, curcuma, Myrrh,Angelica Dahurica,PolygonumCuspidatum, coptis Chinensis,Asarum, Panax Notoginseng,Safflower, Borneol, AgrimoniaPilosa Leaf, Vitex NegundoWhole, Glycerin, Monoglyceride,Petrolatum, Aqua

  • PRINCIPAL DISPLAY PANEL

    12

  • INGREDIENTS AND APPEARANCE
    YOUCOPIA PAIN RELIEF CREAM 
    pain relief cream cream
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:82372-014
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    MENTHOL (UNII: L7T10EIP3A) (MENTHOL - UNII:L7T10EIP3A) MENTHOL0.8 g  in 100 g
    CAMPHOR (NATURAL) (UNII: N20HL7Q941) (CAMPHOR (NATURAL) - UNII:N20HL7Q941) CAMPHOR (NATURAL)0.4 g  in 100 g
    Inactive Ingredients
    Ingredient NameStrength
    POLYGONUM CUSPIDATUM LEAF (UNII: 2540B7G25G)  
    GLYCERYL MONOSTEARATE (UNII: 230OU9XXE4)  
    BORNEOL (UNII: M89NIB437X)  
    PETROLATUM (UNII: 4T6H12BN9U)  
    COPTIS CHINENSIS ROOT (UNII: CXS4LJR7EL)  
    AGRIMONIA PILOSA LEAF (UNII: 6E03WRR337)  
    CURCUMA LONGA (TURMERIC) RHIZOME EXTRACT (UNII: 856YO1Z64F)  
    VITEX NEGUNDO WHOLE (UNII: C92PGK11XB)  
    LIGUSTICUM CHUANXIONG ROOT EXTRACT (UNII: RR83T99U97)  
    MYRRH (UNII: JC71GJ1F3L)  
    ASARUM CAUDATUM ROOT (UNII: 93NNE1H1O7)  
    PANAX NOTOGINSENG ROOT (UNII: GQX1C1175U)  
    SAFFLOWER (UNII: 4VBL71TY4Y)  
    GLYCERIN (UNII: PDC6A3C0OX)  
    WATER (UNII: 059QF0KO0R)  
    ANGELICA DAHURICA ROOT (UNII: 1V63N2S972)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:82372-014-0150 g in 1 TUBE; Type 0: Not a Combination Product11/12/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01711/12/2024
    Labeler - Good Manager Holdings Inc. (118382673)
    Establishment
    NameAddressID/FEIBusiness Operations
    Good Manager Holdings Inc.118382673manufacture(82372-014)
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