Label: HEMORRHOID, FISSURE, PROCTALGIA RELIEF WASH- carbon, panthenol, sodium hyaluronate liquid

  • NDC Code(s): 84533-002-01
  • Packager: WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.
  • Category: HUMAN OTC DRUG LABEL
  • DEA Schedule: None

Drug Label Information

Updated January 14, 2026

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  • ACTIVE INGREDIENT

    Carbon 0.1%
    Panthenol 0.2%
    Sodium Hyaluronate 0.05%
    Glycerin 2%

  • PURPOSE

    Adsorbent and detoxifying
    Healing and barrier protection
    Hydration and wound healing
    Humectant and moisturizing

  • KEEP OUT OF REACH OF CHILDREN

    If swallowed, seek medicalhelp or contact a PoisonControl Center right away.

  • INDICATIONS & USAGE

    instantly helps relieveanorectal itching and discom-fort such as pain, soreness, orburning commonly associatedwith hemorrhoids
    temporarily protects theinflamed, irritated anorectalarea to make future bowelmovements less painful fromirritation and abrasion

  • WARNINGS

    For external use.

  • DOSAGE & ADMINISTRATION

    adults and children 12 yearsof age and over: apply to theaffected area then wash awaywith water and rinse thor-oughly 1-2 times dally orsimply while showering.For intrarectal use: applyaround the affected anal areaand then wash away withwater and rinse thoroughly.
    children under 12 years ofage: ask a doctor

  • STORAGE AND HANDLING

    STAY FRESH,COMFORTABLE,AND CLEAN.

  • INACTIVE INGREDIENT

    Cactus Extract
    Oat Bran Extract
    Ophiopogon Japonicus Root Extract
    Paeonia Lactiflora Root Extract
    Scutellaria Baicalensis Root Extract
    Water
    Sodium Chloride
    DMDM Hydantoin
    Disodium EDTA
    Polyglyceryl-10 Laurate
    Sodium Sulfate
    Butylene Glycol
    Phenoxyethanol
    Lauryl Alcohol

  • PRINCIPAL DISPLAY PANEL

    label1

  • INGREDIENTS AND APPEARANCE
    HEMORRHOID, FISSURE, PROCTALGIA RELIEF WASH 
    carbon, panthenol, sodium hyaluronate liquid
    Product Information
    Product TypeHUMAN OTC DRUGItem Code (Source)NDC:84533-002
    Route of AdministrationTOPICAL
    Active Ingredient/Active Moiety
    Ingredient NameBasis of StrengthStrength
    GLYCERIN (UNII: PDC6A3C0OX) (GLYCERIN - UNII:PDC6A3C0OX) GLYCERIN2 g  in 100 mL
    HYALURONATE SODIUM (UNII: YSE9PPT4TH) (HYALURONIC ACID - UNII:S270N0TRQY) HYALURONATE SODIUM0.05 g  in 100 mL
    PANTHENOL (UNII: WV9CM0O67Z) (PANTHENOL - UNII:WV9CM0O67Z) PANTHENOL0.2 g  in 100 mL
    ACTIVATED CHARCOAL (UNII: 2P3VWU3H10) (ACTIVATED CHARCOAL - UNII:2P3VWU3H10) ACTIVATED CHARCOAL0.1 g  in 100 mL
    Inactive Ingredients
    Ingredient NameStrength
    DMDM HYDANTOIN (UNII: BYR0546TOW)  
    PAEONIA LACTIFLORA ROOT (UNII: 3Z3866YW6P)  
    LAURYL ALCOHOL (UNII: 178A96NLP2)  
    SODIUM CHLORIDE (UNII: 451W47IQ8X)  
    POLYGLYCERYL-10 LAURATE (UNII: MPJ2Q8WI8G)  
    EDETATE DISODIUM (UNII: 7FLD91C86K)  
    SCUTELLARIA BAICALENSIS ROOT (UNII: 7J95K7ID2S)  
    PHENOXYETHANOL (UNII: HIE492ZZ3T)  
    WATER (UNII: 059QF0KO0R)  
    OAT BRAN (UNII: KQX236OK4U)  
    OPUNTIA FICUS-INDICA (UNII: 23Z87HTQ6P)  
    SODIUM SULFATE (UNII: 0YPR65R21J)  
    BUTYLENE GLYCOL (UNII: 3XUS85K0RA)  
    OPHIOPOGON JAPONICUS ROOT (UNII: 90PS6JV9GZ)  
    Packaging
    #Item CodePackage DescriptionMarketing Start DateMarketing End Date
    1NDC:84533-002-01200 mL in 1 BOTTLE; Type 0: Not a Combination Product07/26/2024
    Marketing Information
    Marketing CategoryApplication Number or Monograph CitationMarketing Start DateMarketing End Date
    OTC Monograph DrugM01507/26/2024
    Labeler - WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd. (412779339)
    Establishment
    NameAddressID/FEIBusiness Operations
    WU XI ZHONG ZHI WEI NA TECHNOLOGY CO., Ltd.412779339manufacture(84533-002)
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